A two-step asymmetric synthesis of pure trans-(R,R)-diaryl-epoxides
- 30 June 1996
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (6) , 1783-1788
- https://doi.org/10.1016/0957-4166(96)00213-3
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Chiral sulfur-reagents for the preparation of optically active epoxidesTetrahedron, 1992
- Preparation of optically active epoxides via sulfur ylides. Origin of the chiral induction.Tetrahedron: Asymmetry, 1991
- Preparation of optically active stilbene oxides via sulfonium salts derived from C2 symmetric thiolanes.Tetrahedron Letters, 1990
- Camphoryl sulfide as a chiral auxiliary and a mediator for one-step synthesis of optically active 1,2-diaryloxiranesThe Journal of Organic Chemistry, 1989
- Asymmetric synthesis of trans-2,3-diaryloxiranes. Benzylidene transfer from chiral arsonium ylidesOrganometallics, 1983
- New synthetic methods. Transfer of chirality from sulfur to carbonJournal of the American Chemical Society, 1973
- METHYLENECYCLOHEXANE OXIDEOrganic Syntheses, 1969
- Dimethylsulfonium Methylide, a Reagent for Selective Oxirane Synthesis from Aldehydes and KetonesJournal of the American Chemical Society, 1962
- Dimethylsulfoxonium MethylideJournal of the American Chemical Society, 1962
- The Chemistry of Ylids. VI. Dimethylsulfonium Fluorenylide—A Synthesis of Epoxides1Journal of the American Chemical Society, 1961