Stereoselective reduction of benzoin by the NADH model 3-(dimethylcarbamoyl)-1,2,4-trimethyl-1,4-dihydropyridine
Author:
Publisher
Wiley
Subject
General Chemistry
Reference12 articles.
1. Highly reactive and stereoselective (R)- and (S)-3-(N,N-dimethylcarbamoyl)-1,2,4-trimethyl-1,4-dihydropyridines for NADH-NAD+ mimicry
2. Efficient chirality transfer between a chiral 4-methyl-1,4-dihydropyridine and benzoylformic ester. An example of a pure intermolecular self-immolative process
3. NAD(P)+-NADPH Models. 60. Induction of Double Asymmetry in the Reduction of α-Keto Esters
4. NAD(P)+–NAD(P)H Models. 59. 1,2- Versus 1,4-Reduction of β,γ-Unsaturated α-Keto Ester
5. 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
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