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