Stereoselective synthesis of D(+)-erythro and L(−)-threo sphingosines from carbohydrates

Yadav, J. S. ; Vidyanand, D. ; Rajagopal, D. (1993) Stereoselective synthesis of D(+)-erythro and L(−)-threo sphingosines from carbohydrates Tetrahedron Letters, 34 (7). pp. 1191-1194. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/S0040-4039(00)77525-3

Abstract

Stereocontrolled syntheses of D(+)-erythro and L(−)-threo sphingosines are described starting from D-xylose and D-arabinose respectively through acetylenic intermediates 3 and 4, obtained by base induced double elimination of the β-alkoxy chlorides 5 & 13. Synthesis of the title compounds are described.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:D(+)-erythro and L(−)-threo Sphingosines; Base Induced Double Elimination Reaction; Acetylenic Alcohol
ID Code:58773
Deposited On:02 Sep 2011 03:08
Last Modified:02 Sep 2011 03:08

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