Regioselective ring opening of chiral epoxyalcohols by primary amines
- 18 November 1991
- journal article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 32 (47), 6931-6934
- https://doi.org/10.1016/0040-4039(91)80447-e
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Regioselective ring opening of silyl epoxy alcohols with azide ionTetrahedron Letters, 1990
- Regioselective azide opening of 2,3-epoxy alcohols by [Ti(O-i-Pr)2(N3)2]: synthesis of .alpha.-amino acidsThe Journal of Organic Chemistry, 1988
- Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatizationJournal of the American Chemical Society, 1987
- In situ opening of epoxy alcohols: a convenient alternative to the isolation of unstable epoxy alcoholsThe Journal of Organic Chemistry, 1986
- Regioselective Ring-opening Reactions of 2,3-Epoxy Alcohols with Sodium Azide Supported on Zeolite CaYChemistry Letters, 1986
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- Titanium isopropoxide-mediated nucleophilic openings of 2,3-epoxy alcohols. A mild procedure for regioselective ring-openingThe Journal of Organic Chemistry, 1985
- Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutionsPure and Applied Chemistry, 1983
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969