Neutral solvolysis of covalent arylsulfonylmethyl perchlorates. The kinetic basicity of water and some aliphatic alcohols
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00436a008
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. Medium effects as a criterion for reaction mechanism. Application of the Savage-Wood Additivity of Group Interactions (SWAG) procedures to the mechanism of the neutral hydrolysis of [(p-nitrophenyl)sulfonyl]methyl perchlorate;The Journal of Organic Chemistry;1989-03
2. Water structure and reactivity;Accounts of Chemical Research;1981-06-01
3. α-Oxosulfone, 2. Synthesen von α-Oxosulfonen durch Ozonspaltungen;Liebigs Annalen der Chemie;1979-12-21
4. Stopped-flow study of salt effects on the hydroxide and borate ion catalyzed hydrolysis of covalent p-tolylsulfonylmethyl perchlorate in aqueous borax buffer solutions;The Journal of Organic Chemistry;1978-09
5. ChemInform Abstract: NEUTRAL SOLVOLYSIS OF COVALENT ARYLSULFONYLMETHYL PERCHLORATES. THE KINETIC BASICITY OF WATER AND SOME ALIPHATIC ALCOHOLS;Chemischer Informationsdienst;1977-12-06
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