Stereochemistry of cyclopropane ring opening in the acid-catalyzed fragmentation of -8-tricyclo[3.2.1.02,4]octanone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Action of acid on photothebainehydroquinone: stereochemistry of opening of cyclopropopanes
2. Inversion of configuration in a fused cyclopropane ring opening by hydrochloric acid
3. Synthesis and Solvolytic Reactivity of endo-anti- and endo-syn-8-Tricyclo[3.2.1.02,4]octane Derivatives. Extensive Homoconjugative Participation by a Cyclopropane Ring
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1. Amide-Group-Directed Protonolysis of Cyclopropane: An Approach to 2,2-Disubstituted Pyrrolidines;Organic Letters;2017-04-28
2. Orbital control of stereochemistry in acid-catalysed addition reactions of endo -tricyclo[3.2.1.02,4]0ct-6-ene;Tetrahedron;1984-01
3. Addition of methanol to -tricyclo[3.2.1.02,4]oct-6-ene: a probe of cyclopropyl corner edge protonation;Tetrahedron Letters;1983-01
4. Migration of the methylene bridge during acetolysis of a cyclopropanated -norbornyl brosylate.;Tetrahedron Letters;1976-03
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