Theoretical study of stereoselective reduction controlled by NADH analogs

Journal of Molecular Graphics and Modelling

Volumn 24, Issue 1, 2005, Pages 1-9

  Zhong, Haizhen ^a   Bowen, J Phillip ^a  

^a UNIVERSITY OF NORTH CAROLINA AT GREENSBORO   (United States)

Author keywords

Conformational search; NADH; NADH mimics; Solvent effect; Stereoselectivity

Indexed keywords

CARBOXYLIC ACIDS; ESTERS; POTENTIAL ENERGY;

CONFORMATIONAL SEARCH; NADH; NADH MIMICS; SOLVENT EFFECTS; STEREOSELECTIVITY;

ORGANIC ACIDS;

2 METHYL 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; 2,4 DIMETHYL 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; CARBONYL DERIVATIVE; ENZYME; METHANOL; PYRIDINE DERIVATIVE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; SOLVENT; UNCLASSIFIED DRUG; WATER;

AB INITIO CALCULATION; ARTICLE; CONFORMATION; ENZYME ACTIVITY; GAS; HYDROPHOBICITY; PRIORITY JOURNAL; STEREOCHEMISTRY; THEORETICAL STUDY;

HYDROPHOBICITY; MOLECULAR CONFORMATION; NAD; OXIDATION-REDUCTION; PHASE TRANSITION; SOLVENTS; STEREOISOMERISM; THERMODYNAMICS;

EID: 24944515389     PISSN: 10933263     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmgm.2005.04.003     Document Type: Article

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