Vanadium-catalyzed epoxidations. I. A new selectivity pattern for acyclic allylic alcohols.
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (49) , 4729-4732
- https://doi.org/10.1016/s0040-4039(01)86695-8
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Separation of diastereomers using a low cost preparative medium-pressure liquid chromatographThe Journal of Organic Chemistry, 1979
- Vanadium-catalyzed epoxidation of cyclic allylic alcohols. Stereoselectivity and stereocontrol mechanismJournal of the American Chemical Society, 1979
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- A total synthesis of lasalocid AJournal of the American Chemical Society, 1978
- "Phosphate extension". A strategem for the stereoselective functionalization of acyclic homoallylic alcoholsJournal of the American Chemical Society, 1977
- Mechanism of the molybdenum and vanadium catalyzed epoxidation of olefins by alkyl hydroperoxidesThe Journal of Organic Chemistry, 1977
- Induction asymétrique et cycloadditions[2+1]—IIITetrahedron, 1976
- Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesolJournal of the American Chemical Society, 1974
- Comportement d'hydroperoxydes allyliques a longue chaine en presence de complexes de certains metaux de transition: II. Structure des époxy-alcools formés à partir d'hydroperoxydes d'octadécène-9 oates de méthyle cis et trans en présence d'acétylacétonate de vanadyleChemistry and Physics of Lipids, 1974
- High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxideJournal of the American Chemical Society, 1973