Ketene-forming elimination reactions from aryl phenylacetates promoted by R2NH in MeCN: effects of base-solvent andβ-phenyl group
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference24 articles.
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Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Elimination Reactions of Aryl Furylacetates Promoted by R2 NH in MeCN: Effects of Base Solvent and β-Aryl Group on the Ketene-forming Transition State;Bulletin of the Korean Chemical Society;2017-10-09
2. Elimination Reactions of Aryl Furylacetates Promoted by R2NH-R2NH2+in 70 mol% MeCN(aq). Effects of β-Aryl on the Ketene-Forming Transition-State;Bulletin of the Korean Chemical Society;2014-07-20
3. Elimination Reactions;Organic Reaction Mechanisms Series;2011-08-05
4. Eliminations from aryl bis(p-chlorophenyl)acetates promoted by R2NH in MeCN. Effects of base-solvent and β-aryl group;Kinetics and Catalysis;2009-07
5. Reaction mechanisms : Part (iii) Polar reactions;Annual Reports Section "B" (Organic Chemistry);2008
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