A novel, efficient synthesis of (±)-erythro-sphingosine
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 42 (3) , 917-922
- https://doi.org/10.1016/s0040-4020(01)87498-6
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- A procedure for “iodolactamization”Tetrahedron Letters, 1985
- 1,3-Asymmetric induction: highly stereoselective synthesis of 2,4-trans-disubstituted γ-butyrolactones and γ-butyrothiolactonesJournal of the American Chemical Society, 1984
- A new synthetic approach to 3-amino-1,2-diols from allylic alcohols via trichloroacetimidatesJournal of the Chemical Society, Chemical Communications, 1983
- Stereoselective synthesis of the dihydroxyisoleucine constituent of the amanita mushroom toxinsTetrahedron Letters, 1982
- Regio- and stereocontrolled synthesis of epoxy alcohols and triols from allylic and homoallylic alcohols via iodocarbonatesThe Journal of Organic Chemistry, 1982
- Carbonate extension. A versatile procedure for functionalization of acyclic homoallylic alcohols with moderate stereocontrolThe Journal of Organic Chemistry, 1982
- Stereo- and regiocontrolled synthesis of methyl N-acetyl-.alpha.-D-sibirosaminideJournal of the American Chemical Society, 1982
- Iodo- and Phenylselenocarbamete Cyclizations: New Versatile Methods for Functionalization of Olefinic BondsHETEROCYCLES, 1981
- A new regio- and stereo-selective functionalization of allylic and homoallylic alcoholsJournal of the Chemical Society, Chemical Communications, 1981
- "Phosphate extension". A strategem for the stereoselective functionalization of acyclic homoallylic alcoholsJournal of the American Chemical Society, 1977