Chiral organometallic NADH mimics: Preparation of homochiral (R)-(−)[(η5-c5h5)fe(co)(pph2(o-(l)-menthyl1))]-1-methyl-1,4-dihydronicotinand asymmetric reduction of ethyl benzoylformate.-Reference-Cited by-同舟云学术

Chiral organometallic NADH mimics: Preparation of homochiral (R)-(−)[(η5-c5h5)fe(co)(pph2(o-(l)-menthyl1))]-1-methyl-1,4-dihydronicotinand asymmetric reduction of ethyl benzoylformate.

Published:1990-01 Issue:22 Volume:31 Page:3213-3216
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Davies Stephen G.,Skerlj Renato T.,Whittaker Mark

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Mechanistic models of asymmetric reductions;Ohno,1986

2. Model studies with nicotinamide derivatives

3. Reduction by a model of NAD(P)H. Effect of metal ion and stereochemistry on the reduction of .alpha.-keto esters by 1,4-dihydronicotinamide derivatives

4. Reduction by a model of NAD(P)H. 25. A chiral model which induces high asymmetry

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