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164. ''Carbene Rearrangements XCVII'': "The Carbene Route to ...," in preparation.
164. ''Carbene Rearrangements XCVII'': "The Carbene Route to ...," in preparation.


163. Synthesis and Kinetics of Bicyclo[2.2.0]hexane–1–substituent: Rosenberg, M. G.; Nowienski, A.; Brinker, U. H., in preparation.
163. ''Carbene Rearrangements XCVI'': "Carbene Fidget Spinners: Study of a ...," in preparation.


162. ''Carbene Rearrangements XCVI'': "Carbene Fidget Spinners: Study of a ...," in preparation.
162. "Synthesis of (bicyclo[2.2.0]hex–1–yl)methanal and Arrhenius parameters for thermal rearrangement: radical stabilizing effect of aldehyde substituents on highly strained C–C bonds," Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].


161. ''Carbene Rearrangements XCV'': "Carbene Routes to Cyclopropatetrahedrane," Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.newkai.com/uhb3/images/f/f4/Rosenberg-brinker-2022-carbene-routes-to-cyclopropatetrahedrane-2.pdf ''J. Org. Chem.'' '''2022''', ''87'', 16902 – 16906].  
161. ''Carbene Rearrangements XCV'': "Carbene Routes to Cyclopropatetrahedrane," Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.newkai.com/uhb3/images/f/f4/Rosenberg-brinker-2022-carbene-routes-to-cyclopropatetrahedrane-2.pdf ''J. Org. Chem.'' '''2022''', ''87'', 16902 – 16906].  
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155. "Bromination and Accompanying Rearrangements of the Polycyclic Oxetane 2,4–Oxytwistane," Rosenberg, M. G.; Billing, P.; Brecker, L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo5016129 ''J. Org. Chem.'' '''2014''', ''79'', 8786 – 8799].
155. "Bromination and Accompanying Rearrangements of the Polycyclic Oxetane 2,4–Oxytwistane," Rosenberg, M. G.; Billing, P.; Brecker, L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo5016129 ''J. Org. Chem.'' '''2014''', ''79'', 8786 – 8799].


154. ''Carbene Rearrangements LXXXIX: Carbenes in Constrained Systems XVIII'', “Supramolecular Carbene Chemistry,“ Brinker, U. H.; Mieusset, J.–L.; Rosenberg, M. G. In ''Contemporary Carbene Chemistry,'' Moss, R. A.; Doyle, M. P., Eds., [http://dx.doi.org/10.1002/9781118730379.ch10 Wiley, Hoboken, NJ, USA, 2014, Chapter 10, pp 274 – 323, 4 plates].
154. ''Carbene Rearrangements LXXXIX: Carbenes in Constrained Systems XVIII'', “Supramolecular Carbene Chemistry,“ Brinker, U. H.; Mieusset, J.–L.; Rosenberg, M. G. In ''Contemporary Carbene Chemistry,'' Moss, R. A.; Doyle, M. P., Eds., [http://dx.doi.org/10.1002/9781118730379.ch10 Wiley, Hoboken, NJ, USA, 2014, Chapter 10, pp. 274 – 323, 4 plates].


153. ''Carbene Rearrangements LXXXVIII:'' “Probing the Nature and Extent of Stabilization within Foiled Carbenes: Homoallylic Participation by a Neighboring Cyclopropane Ring,“ Apeland, I. M.; Kählig, H.; Lorbeer, E.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo4004579 ''J. Org. Chem.'' '''2013''', ''78'', 4879 – 4885].
153. ''Carbene Rearrangements LXXXVIII:'' “Probing the Nature and Extent of Stabilization within Foiled Carbenes: Homoallylic Participation by a Neighboring Cyclopropane Ring,“ Apeland, I. M.; Kählig, H.; Lorbeer, E.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo4004579 ''J. Org. Chem.'' '''2013''', ''78'', 4879 – 4885].


152. ''Carbene Rearrangements LXXXVII: Carbenes in Constrained Systems XVII'', “Decomposition of an Oxodiazirine: Free versus Incarcerated Within the Cavities of Two α–Cyclodextrins,“ Mieusset, J.–L.; Thiel, B.; Abraham, M.; Pačar, M.; Brinker, U. H. [https://dx.doi.org/10.1016/j.tetlet.2012.12.008 ''Tetrahedron Lett.'' '''2013''', ''54,'' 681 – 683].
152. ''Carbene Rearrangements LXXXVII: Carbenes in Constrained Systems XVII'', “Decomposition of an Oxodiazirine: Free versus Incarcerated Within the Cavities of Two ''α''–Cyclodextrins,“ Mieusset, J.–L.; Thiel, B.; Abraham, M.; Pačar, M.; Brinker, U. H. [https://dx.doi.org/10.1016/j.tetlet.2012.12.008 ''Tetrahedron Lett.'' '''2013''', ''54,'' 681 – 683].


151. “Mild One-Step Synthesis of Dibromo Compounds from Cyclic Ethers,“ Billing, P.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo302360t ''J. Org. Chem.'' '''2012''', ''77'', 11227 – 11231].
151. “Mild One-Step Synthesis of Dibromo Compounds from Cyclic Ethers,“ Billing, P.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo302360t ''J. Org. Chem.'' '''2012''', ''77'', 11227 – 11231].
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150. “Cucurbit[6]uril as a Potential Catalyst for the Acidic Decomposition of Azidoamines,“ Wieland, M.; Mieusset, J.–L.; Brinker, U. H. [http://dx.doi.org/10.1016/j.tetlet.2012.06.016 ''Tetrahedron Lett.'' '''2012''', ''53,'' 4351 – 4353].
150. “Cucurbit[6]uril as a Potential Catalyst for the Acidic Decomposition of Azidoamines,“ Wieland, M.; Mieusset, J.–L.; Brinker, U. H. [http://dx.doi.org/10.1016/j.tetlet.2012.06.016 ''Tetrahedron Lett.'' '''2012''', ''53,'' 4351 – 4353].


149. ''Carbene Rearrangements LXXXVI: Carbenes in Constrained Systems XVI'', “Cucurbituril Adamantanediazirine Complexes and Consequential Carbene Chemistry,“ Gupta, S.; Choudhury, R.; Krois, D.; Brinker, U. H.*; Ramamurthy, V.* [https://www.newkai.com/uhb3/images/7/79/Cucurbituril.pdf ''J. Org. Chem.'' '''2012''', ''77'', 5155 – 5160]; featured twice in the rotating Highlights on the ''J. Org. Chem.'' home page when published in 2012 and again in May 2013.
149. ''Carbene Rearrangements LXXXVI: Carbenes in Constrained Systems XVI'', “Cucurbituril Adamantanediazirine Complexes and Consequential Carbene Chemistry,“ Gupta, S.; Choudhury, R.; Krois, D.; Brinker, U. H.;* Ramamurthy, V.* [https://www.newkai.com/uhb3/images/7/79/Cucurbituril.pdf ''J. Org. Chem.'' '''2012''', ''77'', 5155 – 5160]; featured twice in the rotating Highlights on the ''J. Org. Chem.'' home page when published in 2012 and again in May 2013.


148. “Solvent Dependency of the Yield of an ''N''–monosubstituted Diaziridine: a GC–MS Study,“ Billing, P.; Brinker, U. H. [http://dx.doi.org/10.1016/j.tetlet.2012.03.105 ''Tetrahedron Lett.'' '''2012''', ''53,'' 2822 – 2824].
148. “Solvent Dependency of the Yield of an ''N''–monosubstituted Diaziridine: a GC–MS Study,“ Billing, P.; Brinker, U. H. [http://dx.doi.org/10.1016/j.tetlet.2012.03.105 ''Tetrahedron Lett.'' '''2012''', ''53,'' 2822 – 2824].


147. ''Carbene Rearrangements LXXXV:'' “Conformations and Reactions of Bicyclo[3.2.1]oct–6–en–8–ylidene,“ Brinker, U. H.; Bespokoev, A. A., Reisenauer, H. P.; Schreiner, P. R. [http://pubs.acs.org/doi/pdf/10.1021/jo3001035 ''J. Org. Chem.'' '''2012''', ''77'', 3800 – 3807]; featured in the rotating Highlights on the ''J. Org. Chem.'' home page.
147. ''Carbene Rearrangements LXXXV:'' “Conformations and Reactions of Bicyclo[3.2.1]oct–6–en–8–ylidene,“ Brinker, U. H.; Bespokoev, A. A.; Reisenauer, H. P.; Schreiner, P. R. [http://pubs.acs.org/doi/pdf/10.1021/jo3001035 ''J. Org. Chem.'' '''2012''', ''77'', 3800 – 3807]; featured in the rotating Highlights on the ''J. Org. Chem.'' home page.


146. ''Carbene Rearrangements LXXXIV:'' “Intra– and Intermolecular Reaction Selectivities of γ–Substituted Adamantanylidenes,“ Knoll, W.; Kaneno, D.; Brecker, L.; Bobek, M. M.; Rosenberg, M. G.; Tomoda, S.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo202132c ''J. Org. Chem.'' '''2012''', ''77'', 1340 – 1360]; featured in the rotating Highlights on the ''J. Org. Chem.'' home page.
146. ''Carbene Rearrangements LXXXIV:'' “Intra– and Intermolecular Reaction Selectivities of γ–Substituted Adamantanylidenes,“ Knoll, W.; Kaneno, D.; Brecker, L.; Bobek, M. M.; Rosenberg, M. G.; Tomoda, S.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo202132c ''J. Org. Chem.'' '''2012''', ''77'', 1340 – 1360]; featured in the rotating Highlights on the ''J. Org. Chem.'' home page.
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145. ''Carbene Rearrangements LXXXIII: Carbenes in Constrained Systems XV'', “Photochemical Generation and Reactivity of Carbenes Within an Organic Cavitand and Capsule: Photochemistry of Adamantanediazirines,“ Gupta, S.; Choudhury, R.; Krois, D.; Wagner, G.; Brinker, U. H.*; Ramamurthy, V.* [https://www.newkai.com/uhb3/images/b/b7/Photochemical_Generation.pdf ''Org. Lett.'' '''2011''', ''13'', 6074 – 6077].
145. ''Carbene Rearrangements LXXXIII: Carbenes in Constrained Systems XV'', “Photochemical Generation and Reactivity of Carbenes Within an Organic Cavitand and Capsule: Photochemistry of Adamantanediazirines,“ Gupta, S.; Choudhury, R.; Krois, D.; Wagner, G.; Brinker, U. H.*; Ramamurthy, V.* [https://www.newkai.com/uhb3/images/b/b7/Photochemical_Generation.pdf ''Org. Lett.'' '''2011''', ''13'', 6074 – 6077].


144. ''Carbene Rearrangements LXXXII:'' “Quest for Even Higher Stabilized Foiled Carbenes,“ Su, K.–J.; Pačar, M.; Mieusset, J.–L.*; Arion, V. B.; Brinker, U. H.* [http://pubs.acs.org/doi/pdf/10.1021/jo201308a ''J. Org. Chem.'' '''2011''', ''76'', 7491 – 7496].
144. ''Carbene Rearrangements LXXXII:'' “Quest for Even Higher Stabilized Foiled Carbenes,“ Su, K.–J.; Pačar, M.; Mieusset, J.–L.;* Arion, V. B.; Brinker, U. H.* [http://pubs.acs.org/doi/pdf/10.1021/jo201308a ''J. Org. Chem.'' '''2011''', ''76'', 7491 – 7496].


143. “Emanuel Vogel (1927 – 2011),“ Altenbach, H.–J.; Brinker, U. H.; Klärner, F. G.; Müllen, K. ''Nachrichten aus der Chemie,'' '''2011''', ''59,'' 655 (in German).
143. “Emanuel Vogel (1927 – 2011),“ Altenbach, H.–J.; Brinker, U. H.; Klärner, F. G.; Müllen, K. ''Nachrichten aus der Chemie,'' '''2011''', ''59,'' 655 (in German).
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140. “Molecular Encapsulation: Organic Reactions in Constrained Systems,“ Brinker, U. H.; Mieusset, J.–L., Eds., [http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470998075.html John Wiley & Sons, Chichester, Great Britain, 2010].
140. “Molecular Encapsulation: Organic Reactions in Constrained Systems,“ Brinker, U. H.; Mieusset, J.–L., Eds., [http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470998075.html John Wiley & Sons, Chichester, Great Britain, 2010].


139. ''Carbene Rearrangements LXXX: Carbenes in Constrained Systems XIV'', “Encapsulation of Reactive Intermediates,“ Mieusset, J.–L.; Brinker, U. H. In “Molecular Encapsulation: Organic Reactions in Constrained Systems,“ Brinker, U. H.; Mieusset, J.–L., Eds.,[http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470998075.html Wiley, Chichester, 2010, Great Britain, pp 269 – 308].
139. ''Carbene Rearrangements LXXX: Carbenes in Constrained Systems XIV'', “Encapsulation of Reactive Intermediates,“ Mieusset, J.–L.; Brinker, U. H. In “Molecular Encapsulation: Organic Reactions in Constrained Systems,“ Brinker, U. H.; Mieusset, J.–L., Eds.,[http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470998075.html Wiley, Chichester, 2010, Great Britain, pp. 269 – 308].


138. “Solvent– and Temperature–Dependent Co–Conformation of Ferrocenyl Azide inside ''β''–Cyclodextrin: Induced Circular Dichroism–, Quantum Mechanical–, and NMR Studies,“ Walla, P.; Brecker, L.; Brinker, U. H., in preparation.
138. “Solvent– and Temperature–Dependent Co–Conformation of Ferrocenyl Azide inside ''β''–Cyclodextrin: Induced Circular Dichroism–, Quantum Mechanical–, and NMR Studies,“ Walla, P.; Brecker, L.; Brinker, U. H., in preparation.
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137. ''Carbene Rearrangements LXXIX:'' “2''H''–Azirines from a Concerted Addition of Alkylcarbenes to Nitrile Groups,“ Knoll, W.; Mieusset, J.–L.; Arion, V. B.; Brecker, L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol100703r ''Org. Lett.'' '''2010''', ''12'', 2366 – 2369].
137. ''Carbene Rearrangements LXXIX:'' “2''H''–Azirines from a Concerted Addition of Alkylcarbenes to Nitrile Groups,“ Knoll, W.; Mieusset, J.–L.; Arion, V. B.; Brecker, L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol100703r ''Org. Lett.'' '''2010''', ''12'', 2366 – 2369].


136. ''Carbene Rearrangements LXXVIII: Carbenes in Constrained Systems XIII'', "Structure–Reactivity Relationships: Reactions of a 5–Substituted Aziadamantane in a Resorcin[4]–arene–based Cavitand,“ Wagner, G.; Knoll, W.; Bobek, M. M.; Brecker, L.; van Herwijnen, H. W. G.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol902667a ''Org. Lett.'' '''2010''', ''12'', 332 – 335].
136. ''Carbene Rearrangements LXXVIII: Carbenes in Constrained Systems XIII'', "Structure–Reactivity Relationships: Reactions of a 5–Substituted Aziadamantane in a Resorcin[4]arene–based Cavitand,“ Wagner, G.; Knoll, W.; Bobek, M. M.; Brecker, L.; van Herwijnen, H. W. G.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol902667a ''Org. Lett.'' '''2010''', ''12'', 332 – 335].


==2005 – 2009==
==2005 – 2009==


135. ''Carbene Rearrangements LXXVII: Carbenes in Constrained Systems XII'', “Supramolecular Photochirogenesis with Carbenes Entrapped in Cyclodextrins,“ Mieusset, J.–L.; Wagner, G.; Su, K.–J.; Steurer, M.; Pačar, M.; Abraham, M.; Brinker, U. H [https://doi.org/10.1002/ejoc.200900899 ''Eur. J. Org. Chem.'' '''2009''', 5907 – 5912].
135. ''Carbene Rearrangements LXXVII: Carbenes in Constrained Systems XII'', “Supramolecular Photochirogenesis with Carbenes Entrapped in Cyclodextrins,“ Mieusset, J.–L.; Wagner, G.; Su, K.–J.; Steurer, M.; Pačar, M.; Abraham, M.; Brinker, U. H. [https://doi.org/10.1002/ejoc.200900899 ''Eur. J. Org. Chem.'' '''2009''', 5907 – 5912].


134. “Controllable Selective Functionalization of a Cavitand via Solid State Photolysis of an Encapsulated Phenyl Azide,“ Wagner, G.; Arion, V. B.; Brecker, L.; Krantz, C.; Mieusset, J.–L.; Brinker, U. H. [https://www.newkai.com/uhb3/images/9/97/Controllable.pdf ''Org. Lett.'' '''2009''', ''11'', 3056 - 3058]; featured in the rotation highlights on the ''Org. Lett.'' home page.
134. “Controllable Selective Functionalization of a Cavitand via Solid State Photolysis of an Encapsulated Phenyl Azide,“ Wagner, G.; Arion, V. B.; Brecker, L.; Krantz, C.; Mieusset, J.–L.; Brinker, U. H. [https://www.newkai.com/uhb3/images/9/97/Controllable.pdf ''Org. Lett.'' '''2009''', ''11'', 3056 - 3058]; featured in the rotation highlights on the ''Org. Lett.'' home page.
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132. ''Carbene Rearrangements LXXVI:'' “Stepwise Insertion of Carbenes into C–H Bonds: The Case of Foiled Carbenes,“ Mieusset, J.–L; Schrems, A.; Abraham, M.; Arion, V. B.; Brinker, U. H. [https://doi.org/10.1016/j.tet.2008.11.063 ''Tetrahedron'', '''2009''', ''65'', 765 – 770].
132. ''Carbene Rearrangements LXXVI:'' “Stepwise Insertion of Carbenes into C–H Bonds: The Case of Foiled Carbenes,“ Mieusset, J.–L; Schrems, A.; Abraham, M.; Arion, V. B.; Brinker, U. H. [https://doi.org/10.1016/j.tet.2008.11.063 ''Tetrahedron'', '''2009''', ''65'', 765 – 770].


131. “Thermal Ring Opening of 1,1–Dibromo– and 1–Bromo–2–chloromethylcyclopropanes: Observation of a Formal Debromochlorination, “ Sydnes, L. K.*; Alnes, K. F.; Pettersen, A.; Brinker, U. H. [https://www.newkai.com/uhb3/images/d/d8/S00706-008-0076-4.pdf ''Monatsh. Chem.'' '''2009''', ''140'', 479 – 483].
131. “Thermal Ring Opening of 1,1–Dibromo– and 1–Bromo–2–chloromethylcyclopropanes: Observation of a Formal Debromochlorination, “ Sydnes, L. K.;* Alnes, K. F.; Pettersen, A.; Brinker, U. H. [https://www.newkai.com/uhb3/images/d/d8/S00706-008-0076-4.pdf ''Monatsh. Chem.'' '''2009''', ''140'', 479 – 483].


130. ''Carbene Rearrangements LXXV:'' “Carbene–Alkene–Complexes between a Nucleophilic Carbene and Electron–Poor Alkenes,“ Mieusset, J.–L; Abraham, M.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ja8042118 ''J. Am. Chem. Soc.'' '''2008''', ''130'', 14634 – 14639].
130. ''Carbene Rearrangements LXXV:'' “Carbene–Alkene–Complexes between a Nucleophilic Carbene and Electron–Poor Alkenes,“ Mieusset, J.–L; Abraham, M.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ja8042118 ''J. Am. Chem. Soc.'' '''2008''', ''130'', 14634 – 14639].
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129. ''Carbene Rearrangements LXXIV:'' “2–Methoxy–Δ<sup>3</sup>–1,3,4–oxadiazoline, a Multipurpose Precursor for the Generation of a Carbene, an Ylide, or a Diazo Compound,“ Mieusset, J.–L; Billing, P.; Abraham, M.; Arion, V. B.; Brecker, L.; Brinker, U. H. [https://doi.org/10.1002/ejoc.200800709 ''Eur. J. Org. Chem.'' '''2008''', 5336 – 5345].
129. ''Carbene Rearrangements LXXIV:'' “2–Methoxy–Δ<sup>3</sup>–1,3,4–oxadiazoline, a Multipurpose Precursor for the Generation of a Carbene, an Ylide, or a Diazo Compound,“ Mieusset, J.–L; Billing, P.; Abraham, M.; Arion, V. B.; Brecker, L.; Brinker, U. H. [https://doi.org/10.1002/ejoc.200800709 ''Eur. J. Org. Chem.'' '''2008''', 5336 – 5345].


128. ''Carbene Rearrangements LXXIII:'' “Substituent Effects on the Ring Opening Mechanism of Lithium Bromocyclopropylidenoids to Allenes,“ Azizoglu, A.*; Balci, M.; Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo8011144 ''J. Org. Chem.'' '''2008''', ''73'', 8182 – 8188].
128. ''Carbene Rearrangements LXXIII:'' “Substituent Effects on the Ring Opening Mechanism of Lithium Bromocyclopropylidenoids to Allenes,“ Azizoglu, A.;* Balci, M.; Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo8011144 ''J. Org. Chem.'' '''2008''', ''73'', 8182 – 8188].


127. ''Carbene Rearrangements LXXII:'' “Intermolecular Reactions of Foiled Carbenes with N–H Bonds: Evidence for an Ylidic Pathway,“ Mieusset, J.–L.; Bespokoev, A.; Pačar, M.; Abraham, M.; Arion, V. B.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo800802m ''J. Org. Chem.'' '''2008''', ''73'', 6551 – 6558].
127. ''Carbene Rearrangements LXXII:'' “Intermolecular Reactions of Foiled Carbenes with N–H Bonds: Evidence for an Ylidic Pathway,“ Mieusset, J.–L.; Bespokoev, A.; Pačar, M.; Abraham, M.; Arion, V. B.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo800802m ''J. Org. Chem.'' '''2008''', ''73'', 6551 – 6558].


126. “Molecular Dynamics Simulation of Configurational Properties of Complexes between β–Cyclodextrin and 2,6–Diaziadamantane in Water, “ Zifferer, G.*; Kornherr, A.; Brinker, U. H. [http://www.tandfonline.com/doi/pdf/10.1080/08927020802193145 ''Molecular Simulation'', '''2008''', ''34'', 1177 – 1183].
126. “Molecular Dynamics Simulation of Configurational Properties of Complexes between β–Cyclodextrin and 2,6–Diaziadamantane in Water,“ Zifferer, G.;* Kornherr, A.; Brinker, U. H. [http://www.tandfonline.com/doi/pdf/10.1080/08927020802193145 ''Molecular Simulation'', '''2008''', ''34'', 1177 – 1183].


125. ''Carbene Rearrangements LXXI:'' “Reactions of Carbenes with Ethers: The Role of Noncovalent Interactions,“ Mieusset, J.–L.; Brinker, U. H. [https://doi.org/10.1002/ejoc.200800256 ''Eur. J. Org. Chem.'' '''2008''', 3363 – 3368].
125. ''Carbene Rearrangements LXXI:'' “Reactions of Carbenes with Ethers: The Role of Noncovalent Interactions,“ Mieusset, J.–L.; Brinker, U. H. [https://doi.org/10.1002/ejoc.200800256 ''Eur. J. Org. Chem.'' '''2008''', 3363 – 3368].


124. ''Carbene Rearrangements LXX:'' “The Carbene Reactivity Surface: A Classification,“ Mieusset, J.–L.*; Brinker, U. H.* [http://pubs.acs.org/doi/pdf/10.1021/jo7026118 ''J. Org. Chem.'' '''2008''', ''73'', 1553 – 1558].
124. ''Carbene Rearrangements LXX:'' “The Carbene Reactivity Surface: A Classification,“ Mieusset, J.–L.;* Brinker, U. H.* [http://pubs.acs.org/doi/pdf/10.1021/jo7026118 ''J. Org. Chem.'' '''2008''', ''73'', 1553 – 1558].


123. “Molecular Dynamics Simulations of ''β''–Cyclodextrin–Aziadamantane Complexes in Water,“ Sellner, B.; Zifferer, G.*; Kornherr, A.; Krois, D.; Brinker, U. H. [https://doi.org/10.1021/jp075493+ ''J. Phys. Chem. B'' '''2008''', ''112'', 710 – 714].
123. “Molecular Dynamics Simulations of ''β''–Cyclodextrin–Aziadamantane Complexes in Water,“ Sellner, B.; Zifferer, G.;* Kornherr, A.; Krois, D.; Brinker, U. H. [https://doi.org/10.1021/jp075493+ ''J. Phys. Chem. B'' '''2008''', ''112'', 710 – 714].


122. ''Carbene Rearrangements LXIX:'' “Toward Selective Reactions with C–H Bonds: A Rationale for the Regio– and Stereochemistry of Dichlorocarbene Insertions into Cyclic Hydrocarbons,“ Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo702047b ''J. Org. Chem.'' '''2007''', ''72'', 10211 – 10219].
122. ''Carbene Rearrangements LXIX:'' “Toward Selective Reactions with C–H Bonds: A Rationale for the Regio– and Stereochemistry of Dichlorocarbene Insertions into Cyclic Hydrocarbons,“ Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo702047b ''J. Org. Chem.'' '''2007''', ''72'', 10211 – 10219].
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116. ''Carbene Rearrangements LXIV: Carbenes in Constrained Systems XI''. Invited Microreview on “Constrained Carbenes,” Rosenberg, M. G.; Brinker U. H. [https://doi.org/10.1002/ejoc.200600547 ''Eur. J. Org. Chem.'' '''2006''', 5423 – 5440].
116. ''Carbene Rearrangements LXIV: Carbenes in Constrained Systems XI''. Invited Microreview on “Constrained Carbenes,” Rosenberg, M. G.; Brinker U. H. [https://doi.org/10.1002/ejoc.200600547 ''Eur. J. Org. Chem.'' '''2006''', 5423 – 5440].


115. “Circular Dichroism of Cyclodextrin Complexes”, Krois, D.; Brinker U. H. In ''Handbook of Cyclodextrins and Their Complexes,'' Dodziuk, H., Ed., [http://dx.doi.org/10.1002/3527608982 Wiley-VCH, Weinheim, 2006, Chapter 10.4, pp 289 – 298].
115. “Circular Dichroism of Cyclodextrin Complexes”, Krois, D.; Brinker U. H. In ''Handbook of Cyclodextrins and Their Complexes,'' Dodziuk, H., Ed., [http://dx.doi.org/10.1002/3527608982 Wiley-VCH, Weinheim, 2006, Chapter 10.4, pp. 289 – 298].


114. ''Carbene Rearrangements LXIII'': “Reactions of ''endo''–3–Diazotricyclo[3.2.1.0<sup>2,4</sup>]oct–6–ene, a Potential Precursor for the Generation of a Neutral C<sub>8</sub>H<sub>8</sub> Molecule with a Pyramidally Coordinated Carbon,” Mieusset, J.–L.; Brinker, U. H. [https://doi.org/10.1021/jo061082y ''J. Org. Chem.'' '''2006''', ''71'', 6975 – 6982].
114. ''Carbene Rearrangements LXIII'': “Reactions of ''endo''–3–Diazotricyclo[3.2.1.0<sup>2,4</sup>]oct–6–ene, a Potential Precursor for the Generation of a Neutral C<sub>8</sub>H<sub>8</sub> Molecule with a Pyramidally Coordinated Carbon,” Mieusset, J.–L.; Brinker, U. H. [https://doi.org/10.1021/jo061082y ''J. Org. Chem.'' '''2006''', ''71'', 6975 – 6982].
Line 115: Line 115:
112. ''Carbene Rearrangements LXII'': “On the Existence of Uncharged Molecules with a Pyramidally Coordinated Carbon: the Cases of Pentacyclo[4.3.0.0<sup>2,9</sup>.0<sup>3,8</sup>.0<sup>7,9</sup>]non-4-ene and Heptacyclo[7.6.0.0<sup>1,5</sup>.0<sup>5,15</sup>.0<sup>6,14</sup>.0<sup>10,14</sup>.0<sup>10,15</sup>]pentadecane,” Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo051847m ''J. Org. Chem.'' '''2005''', ''70'', 10572 – 10575].
112. ''Carbene Rearrangements LXII'': “On the Existence of Uncharged Molecules with a Pyramidally Coordinated Carbon: the Cases of Pentacyclo[4.3.0.0<sup>2,9</sup>.0<sup>3,8</sup>.0<sup>7,9</sup>]non-4-ene and Heptacyclo[7.6.0.0<sup>1,5</sup>.0<sup>5,15</sup>.0<sup>6,14</sup>.0<sup>10,14</sup>.0<sup>10,15</sup>]pentadecane,” Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo051847m ''J. Org. Chem.'' '''2005''', ''70'', 10572 – 10575].


111. ''Carbene Rearrangements LXI: Carbenes in Constrained Systems X'' ,“Carbenes Generated within Cyclodextrins and Zeolites,” Rosenberg, M. G.; Brinker, U. H. In ''Adv. Phys. Org. Chem.'' Richard, J. P., Ed.; Vol. 40, Chapter 1, pp 1 – 47, [http://dx.doi.org/10.1016/s0065-3160(05)40001-5 Academic Press, New York, 2005].
111. ''Carbene Rearrangements LXI: Carbenes in Constrained Systems X'' ,“Carbenes Generated within Cyclodextrins and Zeolites,” Rosenberg, M. G.; Brinker, U. H. In ''Adv. Phys. Org. Chem.,'' Richard, J. P., Ed., [http://dx.doi.org/10.1016/s0065-3160(05)40001-5 Academic Press, New York, 2005, Vol. 40, Chapter 1, pp. 1 – 47].


110. “1–''H''–Cyclobuta[''a'']naphthalen–2–one,” Neudeck, H.; Brinker, U. H. [https://doi.org/10.1016/j.tetlet.2005.01.083 ''Tetrahedron Lett.'' '''2005''', ''46'', 1893 – 1895].
110. “1–''H''–Cyclobuta[''a'']naphthalen–2–one,” Neudeck, H.; Brinker, U. H. [https://doi.org/10.1016/j.tetlet.2005.01.083 ''Tetrahedron Lett.'' '''2005''', ''46'', 1893 – 1895].
Line 129: Line 129:
106. ''Carbene Rearrangements LIX:'' "Regioselective Formation of Alkylidenecyclopropanes from 2–Substituted Cyclobutylidenes Generated from Geminal Dibromocyclobutanes with Methyllithium," Nordvik, T.; Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ol036348r ''Org. Lett.'' '''2004''', ''6'', 715 – 718].
106. ''Carbene Rearrangements LIX:'' "Regioselective Formation of Alkylidenecyclopropanes from 2–Substituted Cyclobutylidenes Generated from Geminal Dibromocyclobutanes with Methyllithium," Nordvik, T.; Mieusset, J.–L.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ol036348r ''Org. Lett.'' '''2004''', ''6'', 715 – 718].


105. “A Novel Route to Geminal Dibromocyclobutanes: Syntheses of 2–Substituted Cyclobutanone Acetals and their Reaction with Boron Tribromide,” Nordvik, T.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo035295o ''J. Org. Chem.'' '''2003''', ''68,'' 9394 – 9399].
105. “A Novel Route to Geminal Dibromocyclobutanes: Syntheses of 2–Substituted Cyclobutanone Acetals and Their Reaction with Boron Tribromide,” Nordvik, T.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo035295o ''J. Org. Chem.'' '''2003''', ''68,'' 9394 – 9399].


104. “Thermolysis of 1–Aryl–Substituted (1,2–Dibromomethylene)cyclopropanes: A Reinvestigation,” Nordvik, T.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo034431m ''J. Org. Chem.'' '''2003''', ''68'', 7092 – 7093].
104. “Thermolysis of 1-(1-Aryl-1-bromomethyl)cyclopropyl Bromides: A Reinvestigation,” Nordvik, T.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo034431m ''J. Org. Chem.'' '''2003''', ''68'', 7092 – 7093].


103. ''Carbene Rearrangements LVIII:'' "Reversal of Diastereoselectivities in Intra– and Intermolecular Reactions of 2–Adamantylidenes Primarily Caused by Electron–Donating and Electron–Withdrawing Substituents on C5,” Knoll, W.; Bobek, M. M.; Kalchhauser, H.; Rosenberg, M. G.; Brinker, U. H. [https://doi.org/10.1021/ol0350700 ''Org. Lett.'' '''2003''', ''5'', 2943 – 2946].
103. ''Carbene Rearrangements LVIII:'' "Reversal of Diastereoselectivities in Intra– and Intermolecular Reactions of 2–Adamantylidenes Primarily Caused by Electron–Donating and Electron–Withdrawing Substituents on C5,” Knoll, W.; Bobek, M. M.; Kalchhauser, H.; Rosenberg, M. G.; Brinker, U. H. [https://doi.org/10.1021/ol0350700 ''Org. Lett.'' '''2003''', ''5'', 2943 – 2946].
Line 139: Line 139:
101. "2,6–Diaziadamantane: A Single Crystal X–ray Diffraction Study and Theoretical Calculations," Bobek, M. M; Krois, D.; Brehmer, T. H.; Giester, G.; Wiberg, K. B.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo020536y ''J. Org. Chem.'' '''2003''', ''68'', 2129 – 2134].
101. "2,6–Diaziadamantane: A Single Crystal X–ray Diffraction Study and Theoretical Calculations," Bobek, M. M; Krois, D.; Brehmer, T. H.; Giester, G.; Wiberg, K. B.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo020536y ''J. Org. Chem.'' '''2003''', ''68'', 2129 – 2134].


100. "Insights into Regioselective Oxy (–O–) and Imino (–NH–) Group Insertions of 3–Nortricyclanone," Rosenberg, M. G., Haslinger, U.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo0159587 ''J. Org. Chem.'' '''2002''', ''67'', 450 – 456].
100. "Insights into Regioselective Oxy (–O–) and Imino (–NH–) Group Insertions of 3–Nortricyclanone," Rosenberg, M. G.; Haslinger, U.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo0159587 ''J. Org. Chem.'' '''2002''', ''67'', 450 – 456].


99. "Probing the Active Catalytic Sites of Zeolites with Benzyl Chloride," van Herwijnen, H. W. G.; Brinker, U. H. [https://doi.org/10.1016/S0040-4020(02)00409-X ''Tetrahedron'' '''2002''''', 58'', 4963 – 4967].
99. "Probing the Active Catalytic Sites of Zeolites with Benzyl Chloride," van Herwijnen, H. W. G.; Brinker, U. H. [https://doi.org/10.1016/S0040-4020(02)00409-X ''Tetrahedron'' '''2002''''', 58'', 4963 – 4967].
Line 151: Line 151:
95. "Synthesis of a Sterically Hindered Diazirine with a Satisfactory Yield: Optically Active 2–Azicamphane“, Krois, D.; Brinker, U. H. [https://doi.org/10.1055/s-2001-11450 ''Synthesis'' '''2001''', 379 – 381].
95. "Synthesis of a Sterically Hindered Diazirine with a Satisfactory Yield: Optically Active 2–Azicamphane“, Krois, D.; Brinker, U. H. [https://doi.org/10.1055/s-2001-11450 ''Synthesis'' '''2001''', 379 – 381].


94. "A Novel and Facile Synthesis of 2,3–Diphenyl–1,3–butadiene," Wagner, R. A.; Brinker, U. H. [https://doi.org/10.1055/s-2001-11448 ''Synthesis'' '''2001''', 376 – 378].
94. "A Novel and Facile Synthesis of 2,3–Diphenyl–1,3–butadiene," Wagner, R. A.; Brinker, U. H. [https://doi.org/10.1055/s-2001-11448 ''Synthesis'' '''2001''', 376 – 378].


93. ''Carbene Rearrangements LV'': "''Carbenes in Constrained Systems. VII'', "Effect of Supramolecular Constraint on the Selectivity of 3–Nortricyclanylidene,“ Rosenberg, M. G., Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo005713e ''J. Org. Chem''. '''2001''', ''66'', 1517 – 1522].
93. ''Carbene Rearrangements LV:'' ''Carbenes in Constrained Systems VII'', "Effect of Supramolecular Constraint on the Selectivity of 3–Nortricyclanylidene," Rosenberg, M. G.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo005713e ''J. Org. Chem''. '''2001''', ''66'', 1517 – 1522].


92. "Induced Circular Dichroism of Cyclodextrin Inclusion Complexes: Examining the Cavity with a Bilateral Probe,“ Bobek, M. M.; Krois, D.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol005923d ''Org. Lett''. '''2000''', ''2'', 1999 – 2002].
92. "Induced Circular Dichroism of Cyclodextrin Inclusion Complexes: Examining the Cavity with a Bilateral Probe,“ Bobek, M. M.; Krois, D.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol005923d ''Org. Lett''. '''2000''', ''2'', 1999 – 2002].


91. ''Carbene Rearrangements LIV'': "Intra- and Intermolecular Diastereoselectivity of 5–Hydroxy–2–adamantylidene. " Bobek, M. M.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ja001123m ''J. Am. Chem. Soc''. '''2000''', ''122'', 7430 – 7431].
91. ''Carbene Rearrangements LIV'': "Intra- and Intermolecular Diastereoselectivity of 5–Hydroxy–2–adamantylidene." Bobek, M. M.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ja001123m ''J. Am. Chem. Soc''. '''2000''', ''122'', 7430 – 7431].


90. "A Sugar–coated Carbene Precursor: A Single Crystal X–ray Diffraction and NMR Study", Bobek, M. M.; Giester, G.; Kählig, H.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)00938-2 ''Tetrahedron Lett''. '''2000''', ''41'', 5663 – 5667].
90. "A 'Sugar–coated' Carbene Precursor: A Single Crystal X–ray Diffraction and NMR Study", Bobek, M. M.; Giester, G.; Kählig, H.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)00938-2 ''Tetrahedron Lett''. '''2000''', ''41'', 5663 – 5667].


89. ''Carbene Rearrangements LIII:'' "Addition of Dichloro– and Dibromocarbene to 1,2–Diphenylcyclobutene,“ Wagner, R. A.; Weber, J.; Brinker, U. H. [http://dx.doi.org/10.1246/cl.2000.246 ''Chemistry Lett''. '''2000''', 246 – 247].
89. ''Carbene Rearrangements LIII:'' "Addition of Dichloro– and Dibromocarbene to 1,2–Diphenylcyclobutene,“ Wagner, R. A.; Weber, J.; Brinker, U. H. [http://dx.doi.org/10.1246/cl.2000.246 ''Chemistry Lett''. '''2000''', 246 – 247].


88. ''Carbene Rearrangements LII:'' "''Carbenes in Constrained Systems. VI'', "Chemospecific Monofunctionalization of ''α''–Cyclodextrin in the Solid State,“ Krois, D.; Bobek, M. M.; Werner, A.; Kählig, H.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol9912635 ''Org. Lett''. '''2000''', ''2'', 315 – 318].
88. ''Carbene Rearrangements LII:'' ''Carbenes in Constrained Systems VI'', "Chemospecific Monofunctionalization of ''α''–Cyclodextrin in the Solid State," Krois, D.; Bobek, M. M.; Werner, A.; Kählig, H.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ol9912635 ''Org. Lett''. '''2000''', ''2'', 315 – 318].


87. "Cyclopropene: A New Simple Synthesis and its Diels–Alder Reaction with Cyclopentadiene“ Binger, P.; Wedemann, P.; Brinker, U. H. [http://dx.doi.org/10.15227/orgsyn.077.0254 ''Org. Synth.'' '''2000''', ''77'', 254 – 259].
87. "Cyclopropene: A New Simple Synthesis and its Diels–Alder Reaction with Cyclopentadiene," Binger, P.; Wedemann, P.; Brinker, U. H. [http://dx.doi.org/10.15227/orgsyn.077.0254 ''Org. Synth.'' '''2000''', ''77'', 254 – 259].


==1995 – 1999==
==1995 – 1999==
Line 171: Line 171:
86. "A Facile One–step Synthesis of 2,4–Adamantanedione," Bobek, M. M.; Brinker, U. H. [https://doi.org/10.1080/00397919908085947 ''Synthetic Commun''. '''1999''', ''29'', 3221 – 3225].
86. "A Facile One–step Synthesis of 2,4–Adamantanedione," Bobek, M. M.; Brinker, U. H. [https://doi.org/10.1080/00397919908085947 ''Synthetic Commun''. '''1999''', ''29'', 3221 – 3225].


85. ''Carbene Rearrangements LI:'' "Competitive Intramolecular Reactions of ''n''–Alkenyl- and ''n''–Alkyl–substituted Cyclopropylidenes: An Insertion Reaction into Non–activated C–H Bonds,” Brinker, U. H.; Miebach, T. [http://pubs.acs.org/doi/abs/10.1021/jo990972t ''J. Org. Chem''. '''1999''', ''64'', 8000 – 8003].
85. ''Carbene Rearrangements LI:'' "Competitive Intramolecular Reactions of ''n''–Alkenyl– and ''n''–Alkyl–substituted Cyclopropylidenes: An Insertion Reaction into Non–activated C–H Bonds,” Brinker, U. H.; Miebach, T. [http://pubs.acs.org/doi/abs/10.1021/jo990972t ''J. Org. Chem''. '''1999''', ''64'', 8000 – 8003].


84. ''Carbene Rearrangements L:'' "1–Bromobicyclo[1.1.0]butane as an Easily Obtainable C4–Building Block: A Novel Route to Cyclobutanone," Weber, J.; Haslinger, U.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo980190k ''J. Org. Chem''. '''1999''', ''64'', 6085 – 6086].
84. ''Carbene Rearrangements L:'' "1–Bromobicyclo[1.1.0]butane as an Easily Obtainable C4–Building Block: A Novel Route to Cyclobutanone," Weber, J.; Haslinger, U.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo980190k ''J. Org. Chem''. '''1999''', ''64'', 6085 – 6086].


83. ''Carbene Rearrangements XLIX:'' "Preparation of 7,7–Dibromobicyclo[4.1.0]heptane," Xu, L.; Brinker, U. H. In "Synthetic Organic Sonochemistry," Luche, J.–L., Ed. [https://doi.org/10.1007/978-1-4899-1910-6_9 Springer, Boston, MA, 1998, 344 – 345].
83. ''Carbene Rearrangements XLIX:'' "Preparation of 7,7–Dibromobicyclo[4.1.0]heptane," Xu, L.; Brinker, U. H. In "Synthetic Organic Sonochemistry," Luche, J.–L., Ed. [https://doi.org/10.1007/978-1-4899-1910-6_9 Springer, Boston, MA, 1998, pp. 344 – 345].


82. "Induced Circular Dichroism and UV–''vis'' Absorption Spectroscopy of Cyclodextrin Inclusion Complexes: Structural Elucidation of Supramolecular Azi–adamantane (Spiro[adamantane–2,3’–diazirine]), " Krois, D.; Brinker. U. H. [http://pubs.acs.org/doi/abs/10.1021/ja982299f ''J. Am. Chem. Soc''., '''1998''', ''120'', 11627 – 11632].
82. "Induced Circular Dichroism and UV–''vis'' Absorption Spectroscopy of Cyclodextrin Inclusion Complexes: Structural Elucidation of Supramolecular Azi–adamantane (Spiro[adamantane–2,3’–diazirine])," Krois, D.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ja982299f ''J. Am. Chem. Soc''., '''1998''', ''120'', 11627 – 11632].


81. ''Advances in Carbene Chemistry'', Vol. 2, Brinker, U. H., Ed. [http://dx.doi.org/10.1021/ja985703j JAI Press, Stamford, CT, USA, 1998].
81. ''Advances in Carbene Chemistry'', Vol. 2, Brinker, U. H., Ed. [http://dx.doi.org/10.1021/ja985703j JAI Press, Stamford, CT, USA, 1998].


80. ''Carbene Rearrangements XLVIII:'' "''Carbenes in Constrained Systems V''. Chemistry of Carbenes in Molecular Reaction Vessels," Brinker, U. H., Rosenberg, M. G. In ''Advances in Carbene Chemistry'', Vol. 2, Brinker, U.H., Ed., [http://dx.doi.org/10.1016/s1079-350x(98)80004-x JAI Press, Stamford, CT, 1998, 29 – 44].
80. ''Carbene Rearrangements XLVIII:'' ''Carbenes in Constrained Systems V''. "Chemistry of Carbenes in Molecular Reaction Vessels," Brinker, U. H., Rosenberg, M. G. In ''Advances in Carbene Chemistry'', Vol. 2, Brinker, U. H., Ed., [http://dx.doi.org/10.1016/s1079-350x(98)80004-x JAI Press, Stamford, CT, 1998, pp. 29 – 44].


79. ''Carbene Rearrangements XLVII:'' "Evidence for a Stepwise Addition of Carbenes to Strained Double Bonds: Reactions of Dihalocarbenes with Cyclopropenes," Weber, J.; Brinker, U. H. [https://doi.org/10.1002/anie.199716231 ''Angew. Chem.'' '''1997''', ''109'', 1689 – 1692]; [https://doi.org/10.1002/anie.199716231 ''Angew. Chem., Int. Ed. Engl.'' '''1997''', ''36'', 1623 – 1626].
79. ''Carbene Rearrangements XLVII:'' "Evidence for a Stepwise Addition of Carbenes to Strained Double Bonds: Reactions of Dihalocarbenes with Cyclopropenes," Weber, J.; Brinker, U. H. [https://doi.org/10.1002/anie.199716231 ''Angew. Chem.'' '''1997''', ''109'', 1689 – 1692]; [https://doi.org/10.1002/anie.199716231 ''Angew. Chem., Int. Ed. Engl.'' '''1997''', ''36'', 1623 – 1626].


78. ''Carbene Rearrangements XLVI:'' "Competing 1,n–Elimination Reactions of 1–Bromo–5–bromomethyl–6,6–dichlorobicyclo[3.1.0]hexane: A Strained 1,3-Bridged Cyclopropene and a Vinylcarbene as Reactive Intermediates," Weber, J.; Brinker, U. H. [https://doi.org/10.1016/0040-4020(96)00912-X ''Tetrahedron'' '''1996''', ''52'', 14641 – 14650].
78. ''Carbene Rearrangements XLVI:'' "Competing 1,n–Elimination Reactions of 1–Bromo–5–bromomethyl–6,6–dichlorobicyclo[3.1.0]hexane: A Strained 1,3–Bridged Cyclopropene and a Vinylcarbene as Reactive Intermediates," Weber, J.; Brinker, U. H. [https://doi.org/10.1016/0040-4020(96)00912-X ''Tetrahedron'' '''1996''', ''52'', 14641 – 14650].


77. "Synthesis of a Sterically Congested Diazirine: 2–Azi–camphane," Kupfer, R.; Rosenberg, M. G.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(96)01497-9 ''Tetrahedron Lett.'' '''1996''', ''37'', 6647 – 6648].
77. "Synthesis of a Sterically Congested Diazirine: 2–Azi–camphane," Kupfer, R.; Rosenberg, M. G.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(96)01497-9 ''Tetrahedron Lett.'' '''1996''', ''37'', 6647 – 6648].
Line 197: Line 197:
73. "A Novel Synthesis of Aromatic ''N''–Chloro Aldimines," Kupfer, R.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo960171f ''J. Org. Chem.'' '''1996''', ''61'', 4185 – 4186].
73. "A Novel Synthesis of Aromatic ''N''–Chloro Aldimines," Kupfer, R.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo960171f ''J. Org. Chem.'' '''1996''', ''61'', 4185 – 4186].


72. ''Carbene Rearrangements XLIV:'' ''"Carbenes in Constrained Systems III.'' Solid State Photolysis of Spirocycloheptane and Spirocyclooctane Diazirine within Cyclodextrins and Zeolites," Kupfer, R.; Brinker, U. H. [https://doi.org/10.1002/jlac.1995199510242 ''(EurJOC) Liebigs Ann.'' '''1995''', 1721 – 1725].
72. ''Carbene Rearrangements XLIV:'' ''Carbenes in Constrained Systems III.'' "Solid State Photolysis of Spirocycloheptane and Spirocyclooctane Diazirine within Cyclodextrins and Zeolites," Kupfer, R.; Brinker, U. H. [https://doi.org/10.1002/jlac.1995199510242 ''(EurJOC) Liebigs Ann.'' '''1995''', 1721 – 1725].


==1990 – 1994==
==1990 – 1994==


71. ''Carbene Rearrangements XLIII: "Carbenes in Constrained Systems II.'' First Carbene Reactions within Zeolites: Solid State Photolysis of Adamantane–2–spiro–3'–diazirine," Kupfer, R.; Poliks, M. D.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ja00095a049 ''J. Am. Chem. Soc.'' '''1994''', ''116'', 7393 – 7398].
71. ''Carbene Rearrangements XLIII: Carbenes in Constrained Systems II.'' First Carbene Reactions within Zeolites: Solid State Photolysis of Adamantane–2–spiro–3'–diazirine," Kupfer, R.; Poliks, M. D.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/ja00095a049 ''J. Am. Chem. Soc.'' '''1994''', ''116'', 7393 – 7398].


70. "Effect of Cyclodextrin on the Intermolecular Photoalkoxycarbonylmethlylation of Anisole," Bantu, N. R.; Kupfer, R.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)77042-0 ''Tetrahedron Lett.'' '''1994''', ''35'', 5117 – 5120].
70. "Effect of Cyclodextrin on the Intermolecular Photoalkoxycarbonylmethlylation of Anisole," Bantu, N. R.; Kupfer, R.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)77042-0 ''Tetrahedron Lett.'' '''1994''', ''35'', 5117 – 5120].
Line 211: Line 211:
67. ''Carbene Rearrangements XLII:'' "Intramolecular Addition ''versus'' Novel Carbon–Hydrogen Bond Insertion Reactions of ''n''–Alkenyl Substituted Cyclopropylidenes," Miebach, T.; Wüster, H.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo00075a067 ''J. Org. Chem.'' '''1993''', ''58'', 6520 – 6523].
67. ''Carbene Rearrangements XLII:'' "Intramolecular Addition ''versus'' Novel Carbon–Hydrogen Bond Insertion Reactions of ''n''–Alkenyl Substituted Cyclopropylidenes," Miebach, T.; Wüster, H.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo00075a067 ''J. Org. Chem.'' '''1993''', ''58'', 6520 – 6523].


66. ''Carbene Rearrangements XLI:'' ''"Carbenes in Constrained Systems I.'' 1,3 Carbon– Hydrogen Bond Insertion Reaction of Adamantylidene within the ''ß''–Cyclodextrin Cavity," Brinker, U. H.; Buchkremer, R.; Kolodziejczyk, M.; Kupfer, R.; Rosenberg, M.; Poliks, M. D.; Orlando, M.; Gross, M. L. [https://doi.org/10.1002/anie.199313441 ''Angew. Chem.'' '''1993''', ''105'', 1427 – 1429]; [https://doi.org/10.1002/anie.199313441 ''Angew. Chem., Int. Ed. Engl.'' '''1993''', ''32,'' 1344 – 1346].
66. ''Carbene Rearrangements XLI:'' ''Carbenes in Constrained Systems I.'' "1,3 Carbon– Hydrogen Bond Insertion Reaction of Adamantylidene within the ''ß''–Cyclodextrin Cavity," Brinker, U. H.; Buchkremer, R.; Kolodziejczyk, M.; Kupfer, R.; Rosenberg, M.; Poliks, M. D.; Orlando, M.; Gross, M. L. [https://doi.org/10.1002/anie.199313441 ''Angew. Chem.'' '''1993''', ''105'', 1427 – 1429]; [https://doi.org/10.1002/anie.199313441 ''Angew. Chem., Int. Ed. Engl.'' '''1993''', ''32,'' 1344 – 1346].


65. "Proton NMR Studies of ''syn''– and ''anti'' –''Tricyclo[5.1.0.0<sup>3,5</sup>]octanes and Their Dichloromethyl Derivatives," Xu, L.; Brinker, U. H.; Smith, W. B. [https://doi.org/10.1002/mrc.1260301208 ''Magn. Reson. Chem.'' '''1992,''' ''30,'' 1196 – 1202].
65. "Proton NMR Studies of ''syn''– and ''anti''–Tricyclo[5.1.0.0<sup>3,5</sup>]octanes and Their Dichloromethyl Derivatives," Xu, L.; Brinker, U. H.; Smith, W. B.   [https://doi.org/10.1002/mrc.1260301208 ''Magn. Reson. Chem.'' '''1992''', ''30'', 1196 – 1202].


64. ''Carbene Rearrangements XL:'' "Efficient Syntheses of Multisubstituted Methylenecyclopropanes via Novel Ultrasonicated Reactions of 1,1–Dihaloolefins and Metals," Xu, L.; Lin, G.; Tao, F.; Brinker, U. H. [http://actachemscand.org/pdf/acta_vol_46_p0650-0653.pdf ''Acta Chem. Scand.'' '''1992''', ''B46'', 650 – 653].
64. ''Carbene Rearrangements XL:'' "Efficient Syntheses of Multisubstituted Methylenecyclopropanes via Novel Ultrasonicated Reactions of 1,1–Dihaloolefins and Metals," Xu, L.; Lin, G.; Tao, F.; Brinker, U. H. [http://actachemscand.org/pdf/acta_vol_46_p0650-0653.pdf ''Acta Chem. Scand.'' '''1992''', ''B46'', 650 – 653].
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58. "Removal of Calcareous Incrustation from Bone and Teeth with Acid and Ultrasound," Stahl, P. W.; Brinker, U. H. [http://www.jstor.org/stable/530161 ''Journal of Field Archaeology,'' '''1991''', ''18'', 138 – 140].
58. "Removal of Calcareous Incrustation from Bone and Teeth with Acid and Ultrasound," Stahl, P. W.; Brinker, U. H. [http://www.jstor.org/stable/530161 ''Journal of Field Archaeology,'' '''1991''', ''18'', 138 – 140].


57. "A Convenient and Improved Technique to Reduce Substantially the Problem of 'Bumping' When Using a Rotary Evaporator, "Buchkremer, R.; Brinker, U. H. [http://jchemed.chem.wisc.edu/Journal/Issues/1990/Dec/jceSubscriber/JCE1990p1071.pdf ''J. Chem. Educ.'' '''1990''', ''67'', 1071].
57. "A Convenient and Improved Technique to Reduce Substantially the Problem of 'Bumping' When Using a Rotary Evaporator," Buchkremer, R.; Brinker, U. H. [http://jchemed.chem.wisc.edu/Journal/Issues/1990/Dec/jceSubscriber/JCE1990p1071.pdf ''J. Chem. Educ.'' '''1990''', ''67'', 1071].


56. ''Carbene Rearrangements XXXVI:'' "Intramolecular Reactions of Diazocyclobutanes. Synthesis of Tricyclo[4.2.0.0<sup>1,3</sup>]octane ([3.5.4]Fenestrane),” Brinker, U. H.; Schrievers, T.; Xu, L. [http://pubs.acs.org/doi/abs/10.1021/ja00179a070 ''J. Am. Chem. Soc.'' '''1990''', ''112'', 8609 – 8611].
56. ''Carbene Rearrangements XXXVI:'' Intramolecular Reactions of Diazocyclobutanes. Synthesis of Tricyclo[4.2.0.0<sup>1,3</sup>]octane ([3.5.4]Fenestrane),” Brinker, U. H.; Schrievers, T.; Xu, L. [http://pubs.acs.org/doi/abs/10.1021/ja00179a070 ''J. Am. Chem. Soc.'' '''1990''', ''112'', 8609 – 8611].


55. ''Festschrift for Wolfgang Kirmse,'' Brinker, U. H., Ed., The State University of New York at Binghamton, Binghamton, NY, USA, 1990.
55. ''Festschrift for Wolfgang Kirmse,'' Brinker, U. H., Ed., The State University of New York at Binghamton, Binghamton, NY, USA, 1990.
Line 243: Line 243:
52. ''Carbene Rearrangements XXXIII:'' "Higher Cycloalkylidenes," Sydnes, L.; Brinker, U. H. In ''Houben–Weyl (Methods in Organic Chemistry)'', Vol. E19b, pp. 601 – 606, Thieme, Stuttgart, 1989 (in German).
52. ''Carbene Rearrangements XXXIII:'' "Higher Cycloalkylidenes," Sydnes, L.; Brinker, U. H. In ''Houben–Weyl (Methods in Organic Chemistry)'', Vol. E19b, pp. 601 – 606, Thieme, Stuttgart, 1989 (in German).


51. ''Carbene Rearrangements XXXII:'' "Cyclohexylidenes, Sydnes, L.; Brinker, U. H. In ''Houben–Weyl (Methods in Organic Chemistry)'', Vol. E19b, pp. 577 – 600, Thieme, Stuttgart, 1989 (in German).
51. ''Carbene Rearrangements XXXII:'' "Cyclohexylidenes," Sydnes, L.; Brinker, U. H. In ''Houben–Weyl (Methods in Organic Chemistry)'', Vol. E19b, pp. 577 – 600, Thieme, Stuttgart, 1989 (in German).


50. ''Carbene Rearrangements XXXI:'' "Cyclopentylidenes," Sydnes, L.; Brinker, U. H. In ''Houben–Weyl (Methods in Organic Chemistry)'', Vol. E19b, pp. 542 – 576, Thieme, Stuttgart, 1989 (in German).
50. ''Carbene Rearrangements XXXI:'' "Cyclopentylidenes," Sydnes, L.; Brinker, U. H. In ''Houben–Weyl (Methods in Organic Chemistry)'', Vol. E19b, pp. 542 – 576, Thieme, Stuttgart, 1989 (in German).
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41. "1,2,4,5-Tetravinylbenzene," Schrievers, T.; Brinker, U. H. [https://www.researchgate.net/publication/235800799_1245-Tetravinylbenzene ''Synthesis'' '''1988,''' 330 – 331].
41. "1,2,4,5-Tetravinylbenzene," Schrievers, T.; Brinker, U. H. [https://www.researchgate.net/publication/235800799_1245-Tetravinylbenzene ''Synthesis'' '''1988,''' 330 – 331].


40. ''Carbene Rearrangements XXIII:'' "Reactions of 2,2,4,4–Tetramethyl–3–methylenecyclobutylidene; Thermal Rearrangements of a 2–Methylenebicyclo[2.1.0]pentane," Brinker, U. H.; Erdle, W. [http://www3.interscience.wiley.com/cgi-bin/abstract/112231978/ABSTRACT ''Angew. Chem.'' '''1987''', ''99,'' 1290 – 1292]; [https://www.academia.edu/20405027/Reactions_of_2_2_4_4-Tetramethyl-3-methylenecyclobutylidene_Thermal_Rearrangements_of_a_2-Methylenebicyclo_2.1.0_pentane ''Angew. Chem., Int. Ed. Engl.'' '''1987''', ''26'', 1260 – 1262].
40. ''Carbene Rearrangements XXIII:'' "Reactions of 2,2,4,4–Tetramethyl–3–methylenecyclobutylidene; Thermal Rearrangements of a 2–Methylenebicyclo[2.1.0]pentane," Brinker, U. H.; Erdle, W. [http://www3.interscience.wiley.com/cgi-bin/abstract/112231978/ABSTRACT ''Angew. Chem.'' '''1987''', ''99,'' 1290 – 1292]; [https://www.newkai.com/uhb3/images/c/ca/Methylenecyclobutylidene_Thermal.pdf ''Angew. Chem., Int. Ed. Engl.'' '''1987''', ''26'', 1260 – 1262].


39. "Dicyclopropa[''a,c'']naphthalene: A Compound Capable of Existence?" Brinker, U. H.; Wüster, H.; Maas, G. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198705771 ''Angew. Chem.'' '''1987,''' ''99'', 585 – 586]; [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198705771 ''Angew. Chem., Int. Ed. Engl.'' '''1987''', ''26'', 577 – 578].
39. "Dicyclopropa[''a,c'']naphthalene: A Compound Capable of Existence?" Brinker, U. H.; Wüster, H.; Maas, G. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198705771 ''Angew. Chem.'' '''1987,''' ''99'', 585 – 586]; [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198705771 ''Angew. Chem., Int. Ed. Engl.'' '''1987''', ''26'', 577 – 578].
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==1980 – 1984==
==1980 – 1984==


31. ''Carbene Rearrangements XVII:'' "Spiro[2.3]hexanes by [4+2]–C–Connection," Brinker, U. H.; Boxberger, M. [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198409741 ''Angew. Chem.'' '''1984,''' ''96'', 971 – 972]; [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198409741 ''Angew. Chem., Int. Ed. Engl.'' '''1984,''' ''23'', 974 – 975].
31. ''Carbene Rearrangements XVII:'' "Spiro[2.3]hexanes by C4 + C2 – Coupling," Brinker, U. H.; Boxberger, M. [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198409741 ''Angew. Chem.'' '''1984,''' ''96'', 971 – 972]; [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198409741 ''Angew. Chem., Int. Ed. Engl.'' '''1984,''' ''23'', 974 – 975].


30. ''Carbene Rearrangements XVI:'' "Bicyclo[3.2.1]octa–2,6–dien–8–ylidene (Homo–7–norbornadienylidene), a 'Foiled' Carbene," Brinker, U. H.; König, L. [https://doi.org/10.1246/cl.1984.45 ''Chem. Lett.'' '''1984''', 45 – 48].
30. ''Carbene Rearrangements XVI:'' "Bicyclo[3.2.1]octa–2,6–dien–8–ylidene (Homo–7–norbornadienylidene), a 'Foiled' Carbene," Brinker, U. H.; König, L. [https://doi.org/10.1246/cl.1984.45 ''Chem. Lett.'' '''1984''', 45 – 48].
Line 294: Line 294:


27. ''Carbene Rearrangements XV:'' "Tricyclo[4.1.0.0<sup>1,3</sup>]hept–4–enes as Intermediates," Brinker, U. H.; Gomann, K; Zorn, R. [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308691 ''Angew. Chem.'' '''1983''', ''95'', 893 – 894];
27. ''Carbene Rearrangements XV:'' "Tricyclo[4.1.0.0<sup>1,3</sup>]hept–4–enes as Intermediates," Brinker, U. H.; Gomann, K; Zorn, R. [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308691 ''Angew. Chem.'' '''1983''', ''95'', 893 – 894];
[https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308691 ''Angew. Chem., Int. Ed. Engl.'' '''1983,''' ''22'', 869 – 870].  
[https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308691 ''Angew. Chem., Int. Ed. Engl.'' '''1983''', ''22'', 869 – 870].  


26. "Thermolysis and Reactions of 4,5–Benzotricyclo[4.1.0.0<sup>1,3</sup>]hept–4–ene and ''o''–(Propadienyl)styrene," Brinker, U. H.; Wilk, G.; Gomann, K. [https://doi.org/10.1002/anie.198312280 ''Angew. Chem. Suppl.'' '''1983''', 1228 – 1239 (in German)].
26. "Thermolysis and Reactions of 4,5–Benzotricyclo[4.1.0.0<sup>1,3</sup>]hept–4–ene and ''o''–(Propadienyl)styrene," Brinker, U. H.; Wilk, G.; Gomann, K. [https://doi.org/10.1002/anie.198312280 ''Angew. Chem. Suppl.'' '''1983''', 1228 – 1239 (in German)].


25. "Thermolysis and Reactions of 4,5–Benzotricyclo[4.1.0.0<sup>1,3</sup>]hept–4–ene and ''o''–(Propadienyl)styrene," Brinker, U. H.; Wilk, G.; Gomann, K. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308681 ''Angew. Chem.'' '''1983''', ''95'', 892 – 893]; [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308681 ''Angew. Chem., Int. Ed. Engl'' '''1983''', ''22,'' 868 – 869].
25. "Thermolysis and Reactions of 4,5–Benzotricyclo[4.1.0.0<sup>1,3</sup>]hept–4–ene and ''o''–(Propadienyl)styrene," Brinker, U. H.; Wilk, G.; Gomann, K. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308681 ''Angew. Chem.'' '''1983''', ''95'', 892 – 893]; [https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198308681 ''Angew. Chem., Int. Ed. Engl.'' '''1983''', ''22,'' 868 – 869].


24. ''Carbene Rearrangements XIV:'' "Regiospecific Rearrangements of Vinyl– and Butadienyl–substituted Cyclopropylidenes," Fleischhauer, I.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)88136-8 ''Tetrahedron Lett.'' '''1983''', ''24'', 3205 – 3208 (in German)].
24. ''Carbene Rearrangements XIV:'' "Regiospecific Rearrangements of Vinyl– and Butadienyl–substituted Cyclopropylidenes," Fleischhauer, I.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)88136-8 ''Tetrahedron Lett.'' '''1983''', ''24'', 3205 – 3208 (in German)].
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23. ''Carbene Rearrangements XIII:'' "Substituted Pyrroles by Carbene–Carbene Rearrangements," Brinker, U. H.; Boxberger, M. [https://www.newkai.com/uhb3/images/4/46/B24-0135.pdf ''J. Chem. Res. (S)'' '''1983''', 100 – 101].
23. ''Carbene Rearrangements XIII:'' "Substituted Pyrroles by Carbene–Carbene Rearrangements," Brinker, U. H.; Boxberger, M. [https://www.newkai.com/uhb3/images/4/46/B24-0135.pdf ''J. Chem. Res. (S)'' '''1983''', 100 – 101].


22. ''Carbene Rearrangements XI:'' "Bicyclo[4.1.1]oct–2–en–7–yliden," Brinker, U. H.; König, L. [https://doi.org/10.1002/cber.19831160308 ''Chem. Ber.'' '''1983''', ''116'', 894 – 910].
22. ''Carbene Rearrangements XI:'' "Bicyclo[4.1.1]oct–2–en–7–yliden," Brinker, U. H.; König, L. [https://doi.org/10.1002/cber.19831160308 ''Chem. Ber.'' '''1983''', ''116'', 894 – 910 (in German)].


21. ''Carbene Rearrangements X:'' "2–Vinylcyclobutyliden," Brinker, U. H.; König, L. [https://doi.org/10.1002/cber.19831160307 ''Chem. Ber.'' '''1983''', ''116'', 882 – 893].
21. ''Carbene Rearrangements X:'' "2–Vinylcyclobutyliden," Brinker, U. H.; König, L. [https://doi.org/10.1002/cber.19831160307 ''Chem. Ber.'' '''1983''', ''116'', 882 – 893 (in German)].


20. ''Carbene Rearrangements XII:'' "''tert''-Butylcarbene from 1,1–Diiodoneopentane," Fukushima, M.; Jones, Jr., M.; Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)87572-3 ''Tetrahedron Lett''. '''1982''', ''23'', 3211 – 3214].
20. ''Carbene Rearrangements XII:'' "''tert''–Butylcarbene from 1,1–Diiodoneopentane," Fukushima, M.; Jones, Jr., M.;* Brinker, U. H. [https://doi.org/10.1016/S0040-4039(00)87572-3 ''Tetrahedron Lett''. '''1982''', ''23'', 3211 – 3214].


19. ''Carbene Rearrangements IX:'' "Cyclobutylidenes from Geminal Dihalogenocyclobutanes," Brinker, U. H.; Schenker, G. [https://pubs.rsc.org/en/content/articlepdf/1982/c3/c39820000679 ''J. Chem. Soc., Chem. Commun.'' '''1982''', 679 – 681].        
19. ''Carbene Rearrangements IX:'' "Cyclobutylidenes from Geminal Dihalogenocyclobutanes," Brinker, U. H.; Schenker, G. [https://www.newkai.com/uhb3/images/8/8c/Cyclobutylidenes_UHB_Schenker.pdf ''J. Chem. Soc., Chem. Commun.'' '''1982''', 679 – 681].      


18. ''Carbene Rearrangements VIII'': "Carbene–Carbene Rearrangements as a Route to 1,5-Dihydropentalene," Brinker, U. H.; Fleischhauer, I. In ''Developments in Polycyclopentanoid Chemistry;'' Paquette, L.A., Ed.; Tetrahedron Symposia-in-Print, [https://doi.org/10.1016/0040-4020(81)80016-6 ''Tetrahedron '''''1981''', ''37'', 4495 – 4502].
18. ''Carbene Rearrangements VIII'': "Carbene–Carbene Rearrangements as a Route to 1,5–Dihydropentalene," Brinker, U. H.; Fleischhauer, I. In ''Developments in Polycyclopentanoid Chemistry;'' Paquette, L. A., Ed.; Tetrahedron Symposia-in-Print, [https://doi.org/10.1016/0040-4020(81)80016-6 ''Tetrahedron '''''1981''', ''37'', 4495 – 4502].


17. ''Carbene Rearrangements VII:'' "Temperature Dependence of Carbene–Carbene Rearrangements. A New Method for the Generation of Carbenes," Brinker, U. H.; Ritzer, J. [http://pubs.acs.org/doi/pdf/10.1021/ja00398a052 ''J. Am. Chem. Soc.'' '''1981''', ''103'', 2116 – 2119].
17. ''Carbene Rearrangements VII:'' "Temperature Dependence of Carbene–Carbene Rearrangements. A New Method for the Generation of Carbenes," Brinker, U. H.; Ritzer, J. [http://pubs.acs.org/doi/pdf/10.1021/ja00398a052 ''J. Am. Chem. Soc.'' '''1981''', ''103'', 2116 – 2119].


16. ''Carbene Rearrangements VI'': "Evidence for a Novel Carbene–Carbene Rearrangement of a New Foiled Methylene, "Brinker, U. H.; König, L. [http://pubs.acs.org/doi/abs/10.1021/ja00391a050 ''J. Am Chem. Soc.'' '''1981''', ''103'', 212 – 214].
16. ''Carbene Rearrangements VI'': "Evidence for a Novel Carbene–Carbene Rearrangement of a New Foiled Methylene," Brinker, U. H.; König, L. [http://pubs.acs.org/doi/abs/10.1021/ja00391a050 ''J. Am. Chem. Soc.'' '''1981''', ''103'', 212 – 214].


15. ''Carbene Rearrangements V:'' "4,5-Benzotricyclo[4.1.0.0<sup>1,3</sup>]hept–4–ene," Brinker, U. H.; Streu, J. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198006311 ''Angew. Chem.'' '''1980''', ''92'', 641 – 642]; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198006311 ''Angew. Chem., Int. Ed. Engl.'' '''1980,''' ''19'', 631 – 632].
15. ''Carbene Rearrangements V:'' "4,5–Benzotricyclo[4.1.0.0<sup>1,3</sup>]hept–4–ene," Brinker, U. H.; Streu, J. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198006311 ''Angew. Chem.'' '''1980''', ''92'', 641 – 642]; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198006311 ''Angew. Chem., Int. Ed. Engl.'' '''1980,''' ''19'', 631 – 632].


14. "Towards a Classification of Singlet Carbenes," Schoeller, W. W.; Brinker, U. H. [https://www.newkai.com/uhb3/images/a/ac/Schoeller%26UHB-ZNat.1980.pdf  ''Z. Naturforsch. - A Journal of Chemical Sciences '''''1980''', ''35b'', 475 – 476].   
14. "Towards a Classification of Singlet Carbenes," Schoeller, W. W.; Brinker, U. H. [https://www.newkai.com/uhb3/images/a/ac/Schoeller%26UHB-ZNat.1980.pdf  ''Z. Naturforsch. - A Journal of Chemical Sciences '''''1980''', ''35 b'', 475 – 476].   


13. ''Carbene Rearrangements IV:'' "1,5-Dihydropentalene by Tandem Carbene–Carbene Rearrangement," Brinker, U. H.; Fleischhauer, I. ; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198003041 ''Angew. Chem.'' '''1980,''' ''92'', 314 – 315]; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198003041 ''Angew. Chem., Int. End. Engl.'' '''1980,''' ''19'', 304 – 305].
13. ''Carbene Rearrangements IV:'' "1,5–Dihydropentalene by Tandem Carbene–Carbene Rearrangement," Brinker, U. H.; Fleischhauer, I. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198003041 ''Angew. Chem.'' '''1980,''' ''92'', 314 – 315]; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198003041 ''Angew. Chem., Int. Ed. Engl.'' '''1980,''' ''19'', 304 – 305].


==1970 – 1979==
==1970 – 1979==


12. ''Carbene Rearrangements III:'' " Carbene Rearrangements of 2–Vinylcyclobutylidene," Brinker, U. H.; König, L. [http://pubs.acs.org/doi/pdf/10.1021/ja00510a055 ''J. Am. Chem. Soc.'' '''1979''', ''101'', 4738 – 4739].
12. ''Carbene Rearrangements III:'' "Carbene Rearrangements of 2–Vinylcyclobutylidene," Brinker, U. H.; König, L. [http://pubs.acs.org/doi/pdf/10.1021/ja00510a055 ''J. Am. Chem. Soc.'' '''1979''', ''101'', 4738 – 4739].


11. ''Carbene Rearrangements II:'' "Carbene–Carbene Rearrangements of ''cis''– and ''trans''–2–(1,3–Butadienyl)cyclopropylidene," Brinker, U. H.; Fleischhauer, I. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961 ''Angew. Chem.'' '''1979''',''91'', 424 – 425]  [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961''Angew. Chem., Int. Ed. Engl.'' '''1979''', ''18'', 396 – 397].
11. ''Carbene Rearrangements II:'' "Carbene–Carbene Rearrangements of ''cis''– and ''trans''–2–(1,3–Butadienyl)cyclopropylidene," Brinker, U. H.; Fleischhauer, I. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961 ''Angew. Chem.'' '''1979''', ''91'', 424 – 425]  [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961''Angew. Chem., Int. Ed. Engl.'' '''1979''', ''18'', 396 – 397].


10. ''Carbene Rearrangements I:'' "On the Thermal Reaction of Vinylcyclopropylidene to Cyclopentenylidene. An Exploration of the Electronic Hypersurface," Schoeller, W. W.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ja00487a006 ''J. Am. Chem. Soc.'' '''1978''', ''100'', 6012 – 6017].
10. ''Carbene Rearrangements I:'' "On the Thermal Reaction of Vinylcyclopropylidene to Cyclopentenylidene. An Exploration of the Electronic Hypersurface," Schoeller, W. W.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/ja00487a006 ''J. Am. Chem. Soc.'' '''1978''', ''100'', 6012 – 6017].
Line 336: Line 336:
8. "Bridged 22π Annulenes from 6,11–Methano[11]annulenylidene," Brinker U. H.; King, R. W.; Jones, W. M. [https://doi.org/10.1021/ja00451a059 ''J. Am. Chem. Soc.'' '''1977''', ''99'', 3175 – 3177].
8. "Bridged 22π Annulenes from 6,11–Methano[11]annulenylidene," Brinker U. H.; King, R. W.; Jones, W. M. [https://doi.org/10.1021/ja00451a059 ''J. Am. Chem. Soc.'' '''1977''', ''99'', 3175 – 3177].


7. "Some Pericyclic Reactions of Carbenes," Jones, W. M.; Brinker, U. H. In: ''Pericyclic Reactions,'' A Series of Monographs: Organic Chemistry [http://dx.doi.org/10.1016/B978-0-12-470501-2.50009-7 Vol. 35, Part 1, Chapter 3, pp. 109 – 198, Marchand, A. P.; Lehr, R. E., Eds., Academic Press: New York, 1977].
7. "Some Pericyclic Reactions of Carbenes," Jones, W. M.; Brinker, U. H. In: ''Pericyclic Reactions,'' A Series of Monographs: Organic Chemistry [http://dx.doi.org/10.1016/B978-0-12-470501-2.50009-7 Vol. 35, Part 1, Marchand, A. P.; Lehr, R. E., Eds., Academic Press: New York, 1977, Chapter 3, pp. 109 – 198].


6. "A Facile Photochemically Induced Arylcarbene–Aromatic Carbene Rearrangement in Solution," Brinker, U. H.; Jones, W. M. [https://doi.org/10.1016/S0040-4039(00)77915-9 ''Tetrahedron Lett.'' '''1976''', ''17'', 577 – 580].
6. "A Facile Photochemically Induced Arylcarbene – Aromatic Carbene Rearrangement in Solution," Brinker, U. H.; Jones, W. M. [https://doi.org/10.1016/S0040-4039(00)77915-9 ''Tetrahedron Lett.'' '''1976''', ''17'', 577 – 580].


5. "2,3–Dichloro–5,6–dicyano–''p''–benzoquinone (DDQ); A New Inexpensive Recovery by Anodic Oxidation of 2,3–Dichloro–5,6–dicyano–''p''–hydroquinone (DDH)," Brinker, U. H.; Tyner III, M.; Jones, W. M. [https://www.researchgate.net/publication/235706637_23-Dichloro-56-dicyano-p-benzoquinone_DDQ_A_New_Inexpensive_Recovery_by_Anodic_Oxidation_of_23-Dichloro-56-dicyano-p-hydroquinone_DDH ''Synthesis'' '''1975''', 671 – 672].
5. "2,3–Dichloro–5,6–dicyano–''p''–benzoquinone (DDQ); A New Inexpensive Recovery by Anodic Oxidation of 2,3–Dichloro–5,6–dicyano–''p''–hydroquinone (DDH)," Brinker, U. H.; Tyner III, M.; Jones, W. M. [https://www.researchgate.net/publication/235706637_23-Dichloro-56-dicyano-p-benzoquinone_DDQ_A_New_Inexpensive_Recovery_by_Anodic_Oxidation_of_23-Dichloro-56-dicyano-p-hydroquinone_DDH ''Synthesis'' '''1975''', 671].


4. "Potential Homoaromatic Compounds with 10 and 14π Electron Systems," Brinker, U. H., Doctoral Dissertation (Dr. rer. nat.), University of Cologne, Federal Republic of Germany, 1973, self-published (in German).
4. "Potential Homoaromatic Compounds with 10 and 14π Electron Systems," Brinker, U. H., Doctoral Dissertation (Dr. rer. nat.), University of Cologne, Federal Republic of Germany, 1973, self-published (in German).


3. "Significance of Stereochemical Factors for the Chemical Shift of the <sup>13</sup>C Resonance," Günther, H.*; Schmickler, H.; Brinker, U. H.; Nachtkamp, K.; Wassen, J.; Vogel, E. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307601 ''Angew. Chem.'' '''1973''', ''85'', 762 – 763] ; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307601 ''Angew. Chem., Int. Ed. Engl.'' '''1973''', ''12'', 760 – 761].
3. "Significance of Stereochemical Factors for the Chemical Shift of the <sup>13</sup>C Resonance," Günther, H.;* Schmickler, H.; Brinker, U. H.; Nachtkamp, K.; Wassen, J.; Vogel, E. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307601 ''Angew. Chem.'' '''1973''', ''85'', 762 – 763] ; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307601 ''Angew. Chem., Int. Ed. Engl.'' '''1973''', ''12'', 760 – 761].


2. "Semibullvalenes as Potential Homoaromatic Compounds," Vogel, E.; Brinker, U. H.; Nachtkamp, K.; Wassen, J.; Müllen, K. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307581 ''Angew. Chem.'' '''1973''', ''85'', 760 – 762]; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307581''Angew. Chem., Int. Ed. Engl.'' '''1973''', ''12'', 758 – 760].
2. "Semibullvalenes as Potential Homoaromatic Compounds," Vogel, E.; Brinker, U. H.; Nachtkamp, K.; Wassen, J.; Müllen, K. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307581 ''Angew. Chem.'' '''1973''', ''85'', 760 – 762]; [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197307581''Angew. Chem., Int. Ed. Engl.'' '''1973''', ''12'', 758 – 760].


1. "Growing of Chalcogenide Single Crystals by Chemical Transport with Aluminum Chloride," Lutz, H. D.*; Lovász, C.; Bertram, K. H.; Srećković, M.; Brinker, U.  
1. "Growing of Chalcogenide Single Crystals by Chemical Transport with Aluminum Chloride," Lutz, H. D.;* Lovász, C.; Bertram, K. H.; Srećković, M.; Brinker, U.  
[https://www.newkai.com/uhb3/images/4/48/BF00910239.pdf ''Monatsh. Chem.'' '''1970''', ''101'', 519 – 524 (in German)].   
[https://www.newkai.com/uhb3/images/4/48/BF00910239.pdf ''Monatsh. Chem.'' '''1970''', ''101'', 519 – 524 (in German)].   




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