Titanium‐Catalyzed Epoxy–Hydroxylation of Allylic Alcohols: A Convenient Diastereoselective Synthesis of Epoxy Diols
- 1 May 1993
- journal article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 32 (5), 733-735
- https://doi.org/10.1002/anie.199307331
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Photooxygenation of chiral allylic alcohols: hydroxy-directed regio- and diastereoselective ene reaction of singlet oxygenJournal of the American Chemical Society, 1992
- Inversion of enantioselectivity in the kinetic resolution mode of the Katsuki-Sharpless asymmetric epoxidation reactionJournal of the American Chemical Society, 1991
- Mechanism of asymmetric epoxidation. 1. KineticsJournal of the American Chemical Society, 1991
- Photooxygenation of olefins in the presence of titanium(IV) catalyst. A convienient "one-pot" synthesis of epoxy alcohols.Journal of the American Chemical Society, 1989
- Regioselective Ene Reaction in the Photooxygenation of Symmetrically Tetrasubstitued Ethenes and the Ti(IV)‐Catalyzed Epoxy‐Hydroxylation of Their Allylic HydroperoxidesEuropean Journal of Inorganic Chemistry, 1988
- A convenient “one-pot” synthesis of epoxy alcohols via photooxygenation of olefins in the presence of titanium(IV) catalystTetrahedron Letters, 1986
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- Stereoselective epoxidation of acyclic allylic alcohols. A correction of our previous work.Tetrahedron Letters, 1979
- Vanadium-catalyzed epoxidations. I. A new selectivity pattern for acyclic allylic alcohols.Tetrahedron Letters, 1979
- Vanadium-catalyzed epoxidation of cyclic allylic alcohols. Stereoselectivity and stereocontrol mechanismJournal of the American Chemical Society, 1979