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X-ray structure determination of a chiral synthon, essential for the synthesis of 25-2H-stigmasterol

Authors :
Marsan, M. P.
Muller, I.
Milon, A.
Warnock, W.
Nakatani, Y.
Ourisson, G.
Jaud, J.
Source :
Journal of Chemical Crystallography; November 1995, Vol. 25 Issue: 11 p783-786, 4p
Publication Year :
1995

Abstract

Synthesis of sterols with varying side chains, including deuterium labeled stigmasterol and sitosterol may be performed via the Wittig-Horner coupling of a 22 aldehyde derived from stigmasterol and a suitable sulfoxide derivative of the side chain. The X-ray structure determination of this synthon have been performed since it is a crucial step in order to know the absolute configuration of the chiral carbon atoms. Crystallographic data were as follows:a=7.437(2),b=10.103(4),c=10.274(3)Å, ß=100.32(6)<superscript>o</superscript>,=759.4 Å<superscript>3</superscript>, space group P2<subscript>1</subscript> (No.4),Z=2,D<subscript>c</subscript>=1.239 g cm<superscript>-3</superscript>.

Details

Language :
English
ISSN :
10741542 and 15728854
Volume :
25
Issue :
11
Database :
Supplemental Index
Journal :
Journal of Chemical Crystallography
Publication Type :
Periodical
Accession number :
ejs15212826
Full Text :
https://doi.org/10.1007/BF01670336