HIGHLY STEREOSELECTIVE SODIUM-BOROHYDRIDE PROMOTED REDUCTION OF TYL-1,2,3,4-TETRACHLORO-7,7-DIMETHOXYNORBORN-2-ENE

Citation
Sg. Bott et al., HIGHLY STEREOSELECTIVE SODIUM-BOROHYDRIDE PROMOTED REDUCTION OF TYL-1,2,3,4-TETRACHLORO-7,7-DIMETHOXYNORBORN-2-ENE, Journal of chemical crystallography, 25(10), 1995, pp. 657-660
Citations number
13
Categorie Soggetti
Crystallography,Spectroscopy
ISSN journal
10741542
Volume
25
Issue
10
Year of publication
1995
Pages
657 - 660
Database
ISI
SICI code
1074-1542(1995)25:10<657:HSSPRO>2.0.ZU;2-N
Abstract
Racemic tyl-1,2,3,4-tetrachloro-7,7-dimethoxynorborn-2-ene was stereos electively reduced by sodium borohydride to give only the S,S or R,R d iastereomers. The crystal structure of the product displays no unusual features.