Reagent dependence of the steric course of bromohydrin and acetoxybromide formation. A case of facile 1,2-interchange in a couple of diastereoisomeric bromohydrins.
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (34) , 3527-3530
- https://doi.org/10.1016/s0040-4039(01)94091-2
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Mise en evidence de l'effet d'angle de torsion dans la serie du tert-butyl-3 cyclohexeneTetrahedron Letters, 1972
- Characterization of torsional angle effects as the dominant steric effect in the hydroxymercuration of substituted cyclohexenesJournal of the American Chemical Society, 1971
- Mechanism of the oxymercuration of substituted cyclohexenesJournal of the American Chemical Society, 1971
- The reactions of methyl hypobromite and acetyl hypobromite with olefinsTetrahedron Letters, 1970
- Derives du -butyl-3 cyclohexene. III.- Les quatre chlorhydrines-trans du -butyl-3 cyclohexeneTetrahedron Letters, 1969
- Stéréochimie de l'époxydation du tert-butyl-3 cyclohexèneCanadian Journal of Chemistry, 1968
- Bromohydrin formation in dimethyl sulfoxideJournal of the American Chemical Society, 1968
- Evaluation of steric effects in additions to substituted cyclohexenesThe Journal of Organic Chemistry, 1968
- Positional selectivity during controlled oxidation of polyolefinsTetrahedron Letters, 1967
- Steroidal Sapogenins. LI. Reaction of Steroidal Olefins with Acetyl Hypobromite2a,bJournal of the American Chemical Society, 1959