NADH mimics on diacetone-d-glucose: Stereoselective biomimetic reduction of benzoylformate and interpretation of chirality transfer deduced by molecular orbital approach-Reference-Cited by-同舟云学术

NADH mimics on diacetone-d-glucose: Stereoselective biomimetic reduction of benzoylformate and interpretation of chirality transfer deduced by molecular orbital approach

Published:1995-06 Issue:23 Volume:51 Page:6459-6474
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Toyooka Yumiko,Matsuzawa Toshihiro,Eguchi Tadashi,Kakinuma Katsumi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference36 articles.

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2. Enzymes in Synthetic Organic Chemistry;Wong,1994

3. Dehydrogenase Requiring Nicotinamide Coenzymes;Jeffery,1980

4. 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

5. NADH mimics for the stereoselective reduction of benzoylformates to the corresponding mandelates.

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4. ChemInform Abstract: Diacetone-Glucose Architecture as a Chirality Template. Part 6. NADH Mimics on Diacetone-D-glucose: Stereoselective Biomimetic Reduction of Benzoylformate and Interpretation of Chirality Transfer Deduced by Molecular Orbital Approach.;ChemInform;2010-08-17

5. Mechanistic Insights on the Magnesium(II) Ion-Activated Reduction of Methyl Benzoylformate with Chelated NADH Peptide β-Lactam Models;The Journal of Organic Chemistry;2009-07-31