Highly enantioselective and regioselective catalytic dihydroxylation of homoallylic alcohol derivatives
- 1 May 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (20) , 3481-3484
- https://doi.org/10.1016/0040-4039(95)00570-3
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Short Enantioselective Synthesis of (-)-Ovalicin, a Potent Inhibitor of Angiogenesis, Using Substrate-Enhanced Catalytic Asymmetric DihydroxylationJournal of the American Chemical Society, 1994
- Catalytic Asymmetric DihydroxylationChemical Reviews, 1994
- A mechanistically designed mono-cinchona alkaloid is an excellent catalyst for the enantioselective dihydroxylation of olefinsTetrahedron Letters, 1994
- X-ray crystallographic studies provide additional evidence that an enzyme-like binding pocket is crucial to the enantioselective dihydroxylation of olefins by OsO4—bis-cinchona alkaloid complexesTetrahedron Letters, 1994
- Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificityJournal of the American Chemical Society, 1993
- The origin of high enantioselectivity in the dihydroxylation of olefins using osmium tetraoxide and cinchona alkaloid catalystsJournal of the American Chemical Society, 1993
- p-Anisyl group: A versatile protecting group for primary alcoholsTetrahedron Letters, 1985