Asymmetric synthesis of polyhydroxylated natural products I. Efficient preparation of L-arabinitol
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (1) , 61-64
- https://doi.org/10.1016/s0040-4039(00)95649-1
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Stereospecific hydroxylation of chiral allylic β-hydroxysulfoxides: Applications to the asymmetric synthesis of optically active vicinal triolsTetrahedron Letters, 1986
- Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxidesTetrahedron Letters, 1985
- La reaction de wittig-horner en milieu heterogene VI1. Selectivite de la reaction sur des composes bifonctionnelsTetrahedron Letters, 1985
- Reduction of .beta.-keto sulfoxides: a highly efficient asymmetric synthesis of both enantiomers of allylic alcoholsThe Journal of Organic Chemistry, 1985
- Synthesis of saccharides and related polyhydroxylated natural products. 3. Efficient conversion of 2,3-erythro-aldoses to 2,3-threo-aldosesJournal of the American Chemical Society, 1982