Effects of Conformation on the Stereochemistry of Solvent Attack on Benzylic β-Hydroxycarbocations: Mechanisms of Epoxide Hydrolysis Reactions-Reference-Cited by-同舟云学术

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Effects of Conformation on the Stereochemistry of Solvent Attack on Benzylic β-Hydroxycarbocations: Mechanisms of Epoxide Hydrolysis Reactions

Published:2006-08-22 Issue:19 Volume:71 Page:7252-7260
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Doan Lanxuan¹,Whalen Dale L.¹

Affiliation:

1. Department of Chemistry, University of Maryland, Baltimore, Maryland 21250

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061003i

Reference17 articles.

1. Enthalpy of vaporization measurements by gas chromatography

2. Trapping of a carbocationic intermediate in the spontaneous hydrolysis reaction of 7.beta.,8.alpha.-dihydroxy-9.beta.,10.beta.-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene: mechanism of the spontaneous and general acid catalyzed hydrolysis reactions of bay-region benzo[a]pyrene 7,8-diol 9,10-epoxides

3. The .alpha.- and .beta.-deuterium isotope effects in the hydrolysis of tetrahydronaphthalene epoxides: rate-limiting hydrogen migration in the spontaneous hydrolysis of 6-methoxy-1,2,3,4-tetrahydronaphthalene oxide

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. Hyperaromatic Stabilization of Arenium Ions: A Remarkable Cis Stereoselectivity of Nucleophilic Trapping of β-Hydroxyarenium Ions by Water;Journal of the American Chemical Society;2011-11-17

2. Carbocations;Organic Reaction Mechanisms · 2006;2010-05-06

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