A new chiral base derived from nicotinamide. Preparation and chiral stability of N,N-dimethyl-2,4-dimethyl-3-carbamoylpyridine in various solvents
Author:
Publisher
Wiley
Subject
General Chemistry
Reference12 articles.
1. Hydride-donation reaction of reduced nicotinamide adenine dinucleotide. 1. MINDO/3 and STO-3G calculations on analog reactions with cyclopropene, tropylidene, and 1,4-dihydropyridine as hydride donors and the cyclopropenium cation as acceptor
2. 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
3. Hydride-abstraction reactions from cycloheptatriene and 1-carbamoylcycloheptatriene. Effect of the CONH2 group orientation on the reactivity difference of the exo and endo hydrogen toward hydride abstraction. A quantum-chemical study
4. A model study of the role of the CONH2-group in the redox Co-enzyme NAD(P)+-NAD(P)H
5. 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
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2. Conformational preference in aromatic amides bearing chiral ortho substituents: its origin and application to relayed stereocontrol;Org. Biomol. Chem.;2006
3. Asymmetric synthesis of axially chiral benzamides and anilides utilizing planar chiral arene chromium complexes;Tetrahedron;2004-05
4. Dynamic resolution of atropisomeric amides using proline-derived imidazolines and ephedrine-derived oxazolidines;Tetrahedron;2004-05
5. Stereodynamics of Bond Rotation in Tertiary Aromatic Amides;Chemistry - A European Journal;2002-03-15
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