Reactions of 4-Nitrophenyl 2-Thiophenecarboxylates with R2NH/R2NH2+in 20 mol % DMSO (aq). Effects of 5-Thienyl Substituent and Base Strength
Author:
Publisher
Korean Chemical Society
Subject
General Chemistry
Link
http://ocean.kisti.re.kr/downfile/crosscheck/chemical/JAKO201321963620253.pdf
Cited by 5 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. 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. 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;Bulletin of the Korean Chemical Society;2019-09-05
4. Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives;Organic Reaction Mechanisms · 2014;2018-01-05
5. Reactions of Aryl 5-substituted-2-Thiophenecarboxylates Promoted by 4-Z-C6H4O−/4-Z-C6H4OH in 20 mol % DMSO(aq). Effect of Nucleophile on Acyl-Transfer Reaction;Bulletin of the Korean Chemical Society;2015-11-25
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