Alkaline Hydrolysis of Y-Substituted Phenyl Phenyl Thionocarbonates: Effect of Changing Electrophilic Center from C=O to C=S on Reactivity and Mechanism
Author:
Publisher
Korean Chemical Society
Subject
General Chemistry
Link
http://ocean.kisti.re.kr/downfile/crosscheck/chemical/JAKO201107049669836.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. Revealing the Hydrolysis Mechanism of a Hg2+-Reactive Fluorescein Probe: Novel Insights on Thionocarbonated Dyes;ACS Omega;2019-12-31
2. Kinetic Study on Nucleophilic Substitution Reactions of O -Phenyl O -Y-substituted-Phenyl Thionocarbonates with 1,8-Diazabicyclo[5.4.0]undec-7-ene in Acetonitrile;Bulletin of the Korean Chemical Society;2017-09-07
3. Experimental and theoretical studies on the nucleofugality ratio in the aminolysis reactions of O-(4-cyanophenyl) O-(3-nitrophenyl) thionocarbonate with amines in aqueous ethanol;New Journal of Chemistry;2017
4. Alkaline Hydrolysis of 4-Nitrophenyl X-Substituted-Benzoates Revisited: New Insights from Yukawa-Tsuno Equation;Bulletin of the Korean Chemical Society;2016-11-17
5. Synthesis of New Artemisinin Analogues from Artemisinic Acid Modified at C-3 and C-13 and Their Antimalarial Activity;Journal of Natural Products;2001-09-01
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