Oxiranylcarbinyl rearrangement: the effect of precursor stereochemistry
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Preferred conformation of the isobutyl, cyclopropylcarbinyl, and oxirylcarbinyl cations, radicals, and anions as determined by semiempirical intermediate neglect of differential orbital calculations
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3. Solvolysis of syn- and anti-9-oxabicyclo[6.1.0]non-2-yl p-bromobenzenesulfonates
4. Evidence for a change in rate-determining step in the acid-catalyzed hydrolysis of a vinyl ether
5. Epoxycarbinyl solvolyses. The solvolytic reactions of syn- and/anti-9-oxabicyclo[6.1.0]non-2-yl p-bromobenzenesulfonates
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3. 13C NMR of 4,5-epoxy-3-substituted decalin and analogous Δ4-octalin derivatives: Epoxide- and methyl-induced shifts;Magnetic Resonance in Chemistry;1994-12
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5. Biomimetic total synthesis of colneleic acid and its function as a lipoxygenase inhibitor;Tetrahedron Letters;1987-01
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