Nicotinamide Adenine Dinucleotide a Unique Compound for Theoretical and Synthetic Model Studies: Chirality as Source for High Stereospecificity
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1081/NCN-120023030
Reference9 articles.
1. 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
2. A new mechanistic model for hydride transfer related to the redox couple NADH/NAD+. Criticism on the quantum-chemical MO approach
3. Highly reactive and stereoselective (R)- and (S)-3-(N,N-dimethylcarbamoyl)-1,2,4-trimethyl-1,4-dihydropyridines for NADH-NAD+ mimicry
4. NADH model mediated reduction of C=N substrates: enantioselective synthesis of D- and L-phenylglycinates
5. NAD(P)+−NAD(P)H Models. 90. Stereoselection Controlled by Electronic Effect of a Carbonyl Group in Oxidation of NAD(P)H Analog
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2. Aromatic interactions at atom-to-atom contact and just beyond: A case study of protein interactions of NAD+/NADP+;International Journal of Biological Macromolecules;2011-12
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5. THE ROLE OF THE CARBOXAMIDE GROUP IN NICOTINAMIDE ADENINE DINUCLEOTIDE IN RELATION TO HYDRIDE TRANSFER: THE REDUCED FORM OF THE DINUCLEOTIDE AS REMEDY IN THE MODULATION OF NEUROTRANSMISSION;Nucleosides, Nucleotides & Nucleic Acids;2005-04-01
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