2,517
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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 John Wiley & Sons, 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]. | ||
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141. ''Carbene Rearrangements LXXXI:'' “Efforts toward Distorted Spiropentanes,“ Su, K.–J.; Mieusset, J.–L.; Arion, V. B.; Knoll, W.; Brecker, L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo1017298 ''J. Org. Chem.'' '''2010''', ''75'', 7494 – 7497]. | 141. ''Carbene Rearrangements LXXXI:'' “Efforts toward Distorted Spiropentanes,“ Su, K.–J.; Mieusset, J.–L.; Arion, V. B.; Knoll, W.; Brecker, L.; Brinker, U. H. [http://pubs.acs.org/doi/pdf/10.1021/jo1017298 ''J. Org. Chem.'' '''2010''', ''75'', 7494 – 7497]. | ||
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 & | 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 John Wiley & Sons, 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. | ||