Reactions of 2,4‐Dinitrophenyl 5‐substituted‐2‐thiophenecarboxylates with R 2 NH/R 2 NH 2 + in 20 Mol % DMSO(aq). Effects of 5‐Thienyl Substituent and Leaving Group on the Reaction Mechanism
Author:
Affiliation:
1. Department of ChemistryPukyong National University Pusan 608‐737 South Korea
2. Department of ChemistryDaejin University Gyeonggi‐do 11159 South Korea
3. Department of ChemistryKorea University Seoul 136‐713 South Korea
Funder
Pukyong National University
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/bkcs.11857
Reference68 articles.
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3. Rates of base-catalysed hydrolysis of substituted aryl benzoates
4. Mechanism of the aminolysis of acetate esters
5. Ingold Lecture. How does a reaction choose its mechanism?
Cited by 2 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. Reactions of 2,4‐dinitrophenyl 5‐substituted‐2‐thiophenecarboxylate promoted by 4‐ZC6H4O−/4‐ZC6H4OH in 20 mol% DMSO(aq). Effects of leaving group and nucleophile on the acyl transfer reactions;Bulletin of the Korean Chemical Society;2023-09
2. 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
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