Elimination Reactions of (E)-2,4-Dinitrobenzaldehyde O-Benzoyloximes Promoted by R2NH/R2NH2+ in 70 mol % MeCN(aq). Change of Reaction Mechanism-Reference-Cited by-同舟云学术

Elimination Reactions of (E)-2,4-Dinitrobenzaldehyde O-Benzoyloximes Promoted by R2NH/R2NH2+ in 70 mol % MeCN(aq). Change of Reaction Mechanism

Published:2008-11-04 Issue:23 Volume:73 Page:9451-9453
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pyun Sang Yong¹,Cho Bong Rae¹

Affiliation:

1. Department of Chemistry, Pukyong National University, Pusan 608-737, Korea, and Department of Chemistry, Korea University, 1-Anamdong, Seoul, 136-701, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo8019412

Reference13 articles.

1. Elimination Reactions of (E)- and (Z)-Benzaldehyde O-Benzoyloximes. Transition State Differences for the Syn- and Anti-Eliminations Forming Nitriles

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

3. Elimination Reactions of (E)- and (Z)-Benzaldehyde O-Pivaloyloximes. Transition-State Differences for the Syn and Anti Eliminations Forming Nitriles

4. Mechanism of Debromination of 1-Aryl-1,2-dibromo-2-nitropropanes Promoted by Secondary Amines in Acetonitrile

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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. Elimination Reactions;Organic Reaction Mechanisms · 2008;2011-08-05

4. Reactions of Aldehydes and Ketones and their Derivatives;Organic Reaction Mechanisms · 2008;2011-08-05

5. Elimination of nitrile from (E)-2,4,6-trinitrobenzaldehyde O-pivaloyloxime promoted by R2NH in MeCN. Effect of β-aryl group on the nitrile-forming transition-state;Kinetics and Catalysis;2011-05