Enantioselective reduction of prochiral ketones using a reagent prepared from lithium aluminium hydride, (+)threo-1,16-dibenzyloxy, 7(R),8(R)- dihydroxy hexadecane and alcohol

Article abstract of DOI:10.1080/00397919808004480

Asytranetric reduction of prochiral ketones to optically active chiral secondary alcohols was achieved using a reagent prepared by modifying lithium aluminium hydride with a chiral auxiliary, (+)threo-1,16-dibenzyloxy,7,8- dihydroxy hexadecane and various

Full text of DOI:10.1080/00397919808004480

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Enantioselective Reduction
of Prochiral Ketones
Using a Reagent Prepared
from Lithium Aluminium
Hydride, (+)Threo-1,16-
Dibenzyloxy, 7(R),8(R)-
Dihydroxy Hexadecane and
Alcohol
N. B. Malkar a & V. G. Kumar a
a Hindustan Lever Research Center , Andheri-
(E), Mumbai, 400099, INDIA
Published online: 23 Aug 2006.
To cite this article: N. B. Malkar & V. G. Kumar (1998) Enantioselective Reduction
of Prochiral Ketones Using a Reagent Prepared from Lithium Aluminium Hydride,
(+)Threo-1,16-Dibenzyloxy, 7(R),8(R)-Dihydroxy Hexadecane and Alcohol,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 28:23, 4445-4461, DOI: 10.1080/00397919808004480
To link to this article: http://dx.doi.org/10.1080/00397919808004480
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