Theoretical study of stereoselective reduction controlled by NADH analogs
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Computer Graphics and Computer-Aided Design,Physical and Theoretical Chemistry,Spectroscopy
Reference17 articles.
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3. Studies on novel and chiral 1,4-dihydropyridines. IV. Mechanistic aspects of the asymmetric reduction with chiral NADH model compounds, (SS)-3-(p-tolylsulfinyl)-1,4-dihydropyridines;Obika;Tetrahedron,1997
4. The hydride-donation reaction of reduced nicotinamide adenine dinucleotide. 2. MINDO/3 and STO-3G calculations on the role of the carbamoyl group in enzymic reactions;Donkersloot;J. Am. Chem. Soc.,1981
5. Theoretical study of conformational features of NAD+ and NADH analogs: protonated nicotinamide and 1,4-dihydronicotinamide;Wu;J. Org. Chem.,1993
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1. Hybrid Quantum and Classical Simulations of the Dihydrofolate Reductase Catalyzed Hydride Transfer Reaction on an Accurate Semi-Empirical Potential Energy Surface;Journal of Chemical Theory and Computation;2011-09-14
2. 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
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