The mechanisms of the oxidation of NADH analogues 2. N-Methyl-substituted 1,4-dihydropyridines
✍ Scribed by A.I. Kruppa; M.B. Taraban; N.E. Polyakov; T.V. Leshina; V. Lūsis; D. Muceniece; G. Duburs
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 480 KB
- Volume
- 73
- Category
- Article
- ISSN
- 1010-6030
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## Abstract The Mg(ClO~4~)~2~‐induced reduction of racemic benzoin by the racemic NADH model compound 3‐(dimethylcarbamoyl)‐1,2,4‐trimethyl‐1,4‐dihydropyridine (1), in accordance to Cram's rule, leads exclusively to __meso__‐1,2‐diphenyl‐1,2‐ethanediol. However, while __R__‐1 equally reduces 5‐benz