Elimination Reactions of (Z)-Thiophene- and (Z)-Furan-2-carbaldehyde O-Benzoyloximes. Effect of β-Aryl Group upon the Nitrile-Forming Anti Transition State
Author:
Affiliation:
1. Department of Chemistry and Center for Electro- & Photo-Responsive Molecules, 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/jo981169m
Reference30 articles.
Cited by 13 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. A Kinetic Study on the Nucleophilic Substitution Reaction of 2,4-dinitrophenyl 5-substituted-2-furoates Under R2NH/R2NH2+in 20 mol% DMSO(aq). Effects of Nonleaving Group and Leaving Group on the Reaction Mechanism;J KOREAN CHEM SOC;2023
2. Reactions of 4‐Nitrophenyl 5‐substituted Furan‐2‐carboxylates with R 2 NH / R 2 NH 2 + in 20 mol% DMSO (aq): Effect of Aryl Group on the Acyl‐Transfer Reaction;Bulletin of the Korean Chemical Society;2021-05-09
3. 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
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. ChemInform Abstract: Elimination Reactions of (Z)-Thiophene- and (Z)-Furan-2-carbaldehyde O-Benzoyloximes. Effect of β-Aryl Group upon the Nitrile-Forming anti Transition State;ChemInform;2010-06-16
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