Reactions of (E)-O-arylbenzaldoximes with secondary amines in acetonitrile. Effect of .beta.-aryl substituents upon the competition between E2 and SNAr reactions
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00075a009
Cited by 12 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. Eliminations from (E)-2,4-Dinitrobenzaldehyde O-Aryloximes Promoted by R3N/R3NH+in 70 mol% MeCN(aq). Effects of Leaving Group and Base-Solvent on the Nitrile-Forming Transition-State;Bulletin of the Korean Chemical Society;2013-04-20
2. Eliminations from (E)-2,4-Dinitrobenzaldehyde O-Aryloximes Promoted by R3N in MeCN. Effects of β-Aryl Group and Base-Solvent on the Nitrile-Forming Transition-State;Bulletin of the Korean Chemical Society;2012-09-20
3. Elimination Reactions of (E)-2,4,6-Trinitrobenzaldehyde O-Aryloximes Promoted by R3N/R3NH+in 70 mol% MeCN(aq). Effect of β-Aryl Group the Nitrile-Forming Transition-State;Bulletin of the Korean Chemical Society;2011-06-20
4. Base-promoted elimination reactions of (E)- and (Z)-arylaldehyde O-benzoyloximes. Effects of stereochemistry, β-aryl group and base-solvent on the nitrile-forming transition states;Arkivoc;2010-07-15
5. ZnO/CH3COCl: A New and Highly Efficient Catalyst for Dehydration of Aldoximes into Nitriles Under Solvent-Free Condition;Synthesis;2005-02-14
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