Rearrangements of Spiropentyl Cation
Author:
Affiliation:
1. Department of Chemistry, Yale University, New Haven, Connecticut 06520-8107
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo990655m
Reference18 articles.
1. Cyclopropyl solvolyses. III. Parent cyclopropyl derivatives and methyl-substituted cyclopropyl tosylates
2. The spiropentyl to 3-methylenecyclobutyl cation rearrangement avoids CH+-trimethylenemethane or the 1-bicyclo[1.1.1]pentyl cation
3. Small-Ring, Spiroalkyl Cations. Solvolysis Studies on 4- and 5-Chlorospirohexane. The Vapor Phase Chlorination of Spirohexane and Spiro [2.4]heptane
4. Formation and Reactions of Bicyclo[1.1.1]pentyl-1 Cations
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