A model study of the role of the CONH2 -group in the redox co-enzyme NAD(P)+ -NAD(P)H. chirality in 2,4-dimethyl-3-carbamoylpyridinium cations
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19821010508/fullpdf
Reference6 articles.
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3. Convergence of active center geometries
4. Pyridine Nucleotide-Dependent Dehydrogenases
5. Notes - Reaction Between Acrolein and Ethyl β-Aminocrotonate
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1. Stereoselective reduction of benzoin by the NADH model 3-(dimethylcarbamoyl)-1,2,4-trimethyl-1,4-dihydropyridine;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. A new chiral base derived from nicotinamide. Preparation and chiral stability of N,N-dimethyl-2,4-dimethyl-3-carbamoylpyridine in various solvents;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. NAD/NADH Models with Axial/Central Chiralities: Superiority of the Quinoline Ring System;The Journal of Organic Chemistry;2001-02-08
4. NAD(P)H-NAD(P)+Models. 73. Structure-Stereochemistry Relationship in the Reaction of NAD Analog;Bulletin of the Chemical Society of Japan;1991-01
5. Reduction of CX to CHXH by Hydride Delivery from Carbon;Comprehensive Organic Synthesis;1991
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