Highly stereoselective synthesis of optically active masked -α,β-dihydroxy aldehydes.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (27) , 3139-3142
- https://doi.org/10.1016/s0040-4039(00)96305-6
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Fumaraldehyde monodimethyl acetal: An easily accessible and versatile intermediate.Tetrahedron Letters, 1986
- ASYMMETRIC OXIDATION OF OLEFINS WITH OSMIUM TETROXIDE COORDINATED BY CHIRAL DIAMINES DERIVED FROM L-TARTARIC ACIDChemistry Letters, 1986
- Asymmetric oxidation of olefins to vicinal diols with osmium tetroxideTetrahedron Letters, 1986
- Asymetric dihydroxylations via chiral oxazolidinesTetrahedron Letters, 1985
- Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic SynthesisAngewandte Chemie International Edition in English, 1985
- Asymmetric induction in the reaction of osmium tetroxide with olefinsJournal of the American Chemical Society, 1980
- Osmium tetraoxide cis hydroxylation of unsaturated substratesChemical Reviews, 1980
- Asymmetric synthesis of nearly optically pure atrolactic acid methyl etherThe Journal of Organic Chemistry, 1979
- Asymmetric Reactions. III. Stereoselectivity Difference between Grignard and Alkyllithium Reactions with 2,3-O-Substituted-d-glyceraldehydesBulletin of the Chemical Society of Japan, 1969
- Synthesis of optically active 1-C-phenylglycerols and their derivativesThe Journal of Organic Chemistry, 1968