The Effect of the Nature of the Leaving Group upon Relative Solvolytic Reactivity1
Author:
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja01463a037
Cited by 16 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. Quantitative structure–conditions–property relationship studies. Neural network modelling of the acid hydrolysis of esters;Mendeleev Communications;2002-01
2. Methanesulfonate/p-nitrobenzoate and p-toluenesulfonate/p-nitrobenzoate rate ratios. Solvolyses of 1-adamantyl and benzhydryl substrates;The Journal of Organic Chemistry;1991-10
3. Solvolyses of diarylmethyl chlorides. A comprehensive stability scale for diarylcarbenium ions.;Tetrahedron;1988-01
4. Solvolyses of aryldineopentylcarbinyl, aryl-tert-butylneopentylcarbinyl, and aryldi-tert-butylcarbinyl p-nitrobenzoates. Effects of the bulky alkyl groups at the reaction center and substituents in the aryl ring;Journal of the American Chemical Society;1973-03
5. Stereochemistry of ion-pair return associated with solvolysis of para-substituted benzyhydryl p-nitrobenzoates;Journal of the American Chemical Society;1971-03
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