Elimination Reactions of (E)-2,4-Dinitrobenzaldehyde O-Benzoyloximes-Reference-Cited by-同舟云学术

Elimination Reactions of (E)-2,4-Dinitrobenzaldehyde O-Benzoyloximes

Published:1999-10-01 Issue:22 Volume:64 Page:8375-8378
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cho Bong Rae¹,Chung Hack Sook¹,Pyun Sang Yong¹

Affiliation:

1. Department of Chemistry and Center for Electro- and Photo-Responsive Molecules, Korea University, 1-Anamdong, Seoul 136-701, Korea, and Department of Chemistry, Pukyong National University, Pusan 608-737, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990752f

Reference23 articles.

1. Eliminations from (E)-O-Arylbenzaldoximes promoted by tertiary amines in acetonitrile. Effects of aryl substituents, base strength, and leaving group upon the nitrile-forming transition state

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1. Elimination Reactions of (E)-2,4,6-TrinitrobenzaldehydeO-Benzoyloximes Promoted by R2NH/R2NH2+in 70 mol% MeCN (aq). Effects of the β-Aryl Group and Leaving Group on Nitrile-Forming Transition States;Bulletin of the Korean Chemical Society;2016-05-27

2. 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

3. 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

4. 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

5. 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