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	<id>https://www.newkai.com/uhb3/index.php?action=history&amp;feed=atom&amp;title=Publications</id>
	<title>Publications - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://www.newkai.com/uhb3/index.php?action=history&amp;feed=atom&amp;title=Publications"/>
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	<updated>2026-06-03T15:33:33Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4281&amp;oldid=prev</id>
		<title>Ubrinker: /* 1990 – 1994 */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4281&amp;oldid=prev"/>
		<updated>2026-05-20T19:10:11Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;1990 – 1994&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
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				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 19:10, 20 May 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l233&quot;&gt;Line 233:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 233:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;59. &amp;quot;The Reaction of Cyclopropabenzene with 1,3–Diphenylisobenzofuran: Formal [4π + 2π] and [4π + 2σ] Cycloadditions,&amp;quot; Brinker, U. H.; Wüster, H. [https://doi.org/10.1016/S0040-4039(00)74835-0 ''Tetrahedron Lett.'' '''1991''', ''32'', 593 – 596].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;59. &amp;quot;The Reaction of Cyclopropabenzene with 1,3–Diphenylisobenzofuran: Formal [4π + 2π] and [4π + 2σ] Cycloadditions,&amp;quot; Brinker, U. H.; Wüster, H. [https://doi.org/10.1016/S0040-4039(00)74835-0 ''Tetrahedron Lett.'' '''1991''', ''32'', 593 – 596].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;58. News and Short Contributions: &amp;quot;Petrographic Thin Sections and the Development of Neolithic Plaster Production in Northern Israel,&amp;quot; Goren, Y.; Goldberg, P. and &amp;quot;Removal of Calcareous Incrustation from Bone and Teeth with Acid and Ultrasound,&amp;quot; Stahl, P. W.; Brinker, U. H. [http://www.jstor.org/stable/530161 ''Journal of Field Archaeology,'' '''1991''', ''18'', 138 – 140].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;58. News and Short Contributions: &amp;quot;Petrographic Thin Sections and the Development of Neolithic Plaster Production in Northern Israel,&amp;quot; Goren, Y.; Goldberg, P. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt; &lt;/ins&gt;and &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt; &lt;/ins&gt;&amp;quot;Removal of Calcareous Incrustation from Bone and Teeth with Acid and Ultrasound,&amp;quot; Stahl, P. W.; Brinker, U. H. [http://www.jstor.org/stable/530161 ''Journal of Field Archaeology,'' '''1991''', ''18'', 138 – 140].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;57. &amp;quot;A Convenient and Improved Technique to Reduce Substantially the Problem of 'Bumping' When Using a Rotary Evaporator,&amp;quot; Buchkremer, R.; Brinker, U. H. [http://jchemed.chem.wisc.edu/Journal/Issues/1990/Dec/jceSubscriber/JCE1990p1071.pdf ''J. Chem. Educ.'' '''1990''', ''67'', 1071].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;57. &amp;quot;A Convenient and Improved Technique to Reduce Substantially the Problem of 'Bumping' When Using a Rotary Evaporator,&amp;quot; Buchkremer, R.; Brinker, U. H. [http://jchemed.chem.wisc.edu/Journal/Issues/1990/Dec/jceSubscriber/JCE1990p1071.pdf ''J. Chem. Educ.'' '''1990''', ''67'', 1071].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4280&amp;oldid=prev</id>
		<title>Ubrinker: /* 1990 – 1994 */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4280&amp;oldid=prev"/>
		<updated>2026-05-20T19:08:19Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;1990 – 1994&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 19:08, 20 May 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l233&quot;&gt;Line 233:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 233:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;59. &amp;quot;The Reaction of Cyclopropabenzene with 1,3–Diphenylisobenzofuran: Formal [4π + 2π] and [4π + 2σ] Cycloadditions,&amp;quot; Brinker, U. H.; Wüster, H. [https://doi.org/10.1016/S0040-4039(00)74835-0 ''Tetrahedron Lett.'' '''1991''', ''32'', 593 – 596].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;59. &amp;quot;The Reaction of Cyclopropabenzene with 1,3–Diphenylisobenzofuran: Formal [4π + 2π] and [4π + 2σ] Cycloadditions,&amp;quot; Brinker, U. H.; Wüster, H. [https://doi.org/10.1016/S0040-4039(00)74835-0 ''Tetrahedron Lett.'' '''1991''', ''32'', 593 – 596].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;58. &amp;quot;Removal of Calcareous Incrustation from Bone and Teeth with Acid and Ultrasound,&amp;quot; Stahl, P. W.; Brinker, U. H. [http://www.jstor.org/stable/530161 ''Journal of Field Archaeology,'' '''1991''', ''18'', 138 – 140].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;58. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;News and Short Contributions: &amp;quot;Petrographic Thin Sections and the Development of Neolithic Plaster Production in Northern Israel,&amp;quot; Goren, Y.; Goldberg, P. and &lt;/ins&gt;&amp;quot;Removal of Calcareous Incrustation from Bone and Teeth with Acid and Ultrasound,&amp;quot; Stahl, P. W.; Brinker, U. H. [http://www.jstor.org/stable/530161 ''Journal of Field Archaeology,'' '''1991''', ''18'', 138 – 140].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;57. &amp;quot;A Convenient and Improved Technique to Reduce Substantially the Problem of 'Bumping' When Using a Rotary Evaporator,&amp;quot; Buchkremer, R.; Brinker, U. H. [http://jchemed.chem.wisc.edu/Journal/Issues/1990/Dec/jceSubscriber/JCE1990p1071.pdf ''J. Chem. Educ.'' '''1990''', ''67'', 1071].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;57. &amp;quot;A Convenient and Improved Technique to Reduce Substantially the Problem of 'Bumping' When Using a Rotary Evaporator,&amp;quot; Buchkremer, R.; Brinker, U. H. [http://jchemed.chem.wisc.edu/Journal/Issues/1990/Dec/jceSubscriber/JCE1990p1071.pdf ''J. Chem. Educ.'' '''1990''', ''67'', 1071].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4274&amp;oldid=prev</id>
		<title>Ubrinker: /* 2020 – Present */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4274&amp;oldid=prev"/>
		<updated>2026-04-27T13:43:10Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;2020 – Present&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 13:43, 27 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://pubs.acs.org/doi/10.1021/acs.joc.5c03248 ''J. Org. Chem.'' '''2026''', ''91'', 5699 – &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;5705&lt;/del&gt;].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://pubs.acs.org/doi/10.1021/acs.joc.5c03248 ''J. Org. Chem.'' '''2026''', ''91'', 5699 – &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;5704&lt;/ins&gt;].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4273&amp;oldid=prev</id>
		<title>Ubrinker: /* 2020 – Present */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4273&amp;oldid=prev"/>
		<updated>2026-04-26T14:56:47Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;2020 – Present&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 14:56, 26 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-notice&quot; lang=&quot;en&quot;&gt;&lt;div class=&quot;mw-diff-empty&quot;&gt;(No difference)&lt;/div&gt;
&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4272&amp;oldid=prev</id>
		<title>Ubrinker: /* 2020 – Present */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4272&amp;oldid=prev"/>
		<updated>2026-04-26T14:56:47Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;2020 – Present&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 14:56, 26 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://pubs.acs.org/doi/10.1021/acs.joc.5c03248 ''J. Org. Chem.'' '''2026''', ''91'', &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;XXX &lt;/del&gt;– &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;XXX&lt;/del&gt;].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://pubs.acs.org/doi/10.1021/acs.joc.5c03248 ''J. Org. Chem.'' '''2026''', ''91'', &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;5699 &lt;/ins&gt;– &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;5705&lt;/ins&gt;].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4261&amp;oldid=prev</id>
		<title>Ubrinker: /* 2020 – Present */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4261&amp;oldid=prev"/>
		<updated>2026-04-15T12:41:37Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;2020 – Present&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 12:41, 15 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://pubs.acs.org/doi/10.1021/acs.joc.5c03248&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;.pdf.&lt;/del&gt;''J. Org. Chem.'' '''2026''', ''91'', XXX – XXX].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://pubs.acs.org/doi/10.1021/acs.joc.5c03248 ''J. Org. Chem.'' '''2026''', ''91'', XXX – XXX].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4260&amp;oldid=prev</id>
		<title>Ubrinker: /* 2020 – Present */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4260&amp;oldid=prev"/>
		<updated>2026-04-15T12:39:25Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;2020 – Present&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 12:39, 15 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;doi&lt;/del&gt;.org/10.1021/acs.joc.5c03248.pdf ''J. Org. Chem.'' '''2026''', ''91'', XXX – XXX].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;pubs.acs&lt;/ins&gt;.org&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;/doi&lt;/ins&gt;/10.1021/acs.joc.5c03248.pdf&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;.&lt;/ins&gt;''J. Org. Chem.'' '''2026''', ''91'', XXX – XXX].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4257&amp;oldid=prev</id>
		<title>Ubrinker: /* 2020 – Present */</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4257&amp;oldid=prev"/>
		<updated>2026-04-07T21:29:25Z</updated>

		<summary type="html">&lt;p&gt;&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;2020 – Present&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 21:29, 7 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://doi.org/10.1021/acs.joc.5c03248.pdf ''J. Org. Chem.'' '''2026''', ''91'', &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;0000 &lt;/del&gt;– &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt; 0000&lt;/del&gt;].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess''' [https://doi.org/10.1021/acs.joc.5c03248.pdf ''J. Org. Chem.'' '''2026''', ''91'', &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;XXX &lt;/ins&gt;– &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;XXX&lt;/ins&gt;].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4256&amp;oldid=prev</id>
		<title>Ubrinker at 22:04, 6 April 2026</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4256&amp;oldid=prev"/>
		<updated>2026-04-06T22:04:05Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 22:04, 6 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt; &lt;/del&gt;Brinker, U. H., '''OpenAccess''' [https://doi.org/10.1021/acs.joc.5c03248.pdf ''J. Org. Chem.'' '''2026''', ''91'', &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;A &lt;/del&gt;– &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;F&lt;/del&gt;].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Rosenberg, M. G.&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;; &lt;/ins&gt;Brinker, U. H., '''OpenAccess''' [https://doi.org/10.1021/acs.joc.5c03248.pdf ''J. Org. Chem.'' '''2026''', ''91'', &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;0000 &lt;/ins&gt;– &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt; 0000&lt;/ins&gt;].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
	<entry>
		<id>https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4255&amp;oldid=prev</id>
		<title>Ubrinker at 21:58, 6 April 2026</title>
		<link rel="alternate" type="text/html" href="https://www.newkai.com/uhb3/index.php?title=Publications&amp;diff=4255&amp;oldid=prev"/>
		<updated>2026-04-06T21:58:44Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 21:58, 6 April 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l11&quot;&gt;Line 11:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 11:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;164. ''Carbene Rearrangements XCVII'': &amp;quot;Competitive Formation of 1,4– and 1,6–Dihydropentalenes via Foiled Reaction Carbene ...&amp;quot; in preparation.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; Brinker, U. H., '''OpenAccess''' [https://doi.org/10.1021/acs.joc.5c03248 &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Rosenberg, M. G&lt;/del&gt;. ''J. Org. Chem.'' '''2026''', ''91'', &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;0000 &lt;/del&gt;– &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt; 0000&lt;/del&gt;].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;163. ''Carbene Rearrangements XCVI'': &amp;quot;Quest for 2,3-Secopyramidane: Computations Hint at Elusive Structure during Skattebøl Rearrangement of Vinylcyclopropylidene,&amp;quot; &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Rosenberg, M. G.&amp;lt; &lt;/ins&gt;Brinker, U. H., '''OpenAccess''' [https://doi.org/10.1021/acs.joc.5c03248.&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;pdf &lt;/ins&gt;''J. Org. Chem.'' '''2026''', ''91'', &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;A &lt;/ins&gt;– &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;F&lt;/ins&gt;].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;162. &amp;quot;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,&amp;quot; Nowienski, A.; Rosenberg, M. G.; Brinker, U. H., '''OpenAccess'''  [https://www.sciencedirect.com/science/article/pii/S0040403924004647/pdfft?md5=b1f0ea342cec97036c8a4b1bfbd42f4b&amp;amp;pid=1-s2.0-S0040403924004647-main.pdf ''Tetrahedron Lett.'' '''2024''', ''153'', 155369 (pp. 1 – 5)].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Ubrinker</name></author>
	</entry>
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