𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Kinetic and mechanistic investigation on
✍ Bingjun Zhao; Xiaoqing Zhu; Yun Lu; Chi-Zhong Xia; Jin-Pei Cheng 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 98 KB

The reaction kinetics of the reactions of Hantzsch esters (HEH) and Hantzsch 4-aryl-1,4-dihydropyridines (4aryl-HEH) with the tropylium cation as a formal hydride acceptor were investigated. The observed kinetic isotope effect (KIE, k H /k D ), using HEH and 4,4-d 2 -HEH as substrates, was 4.16, sug

Stereoselective reduction of benzoin by
✍ Nicoline A. Beijer; Jozef A. J. M. Vekemans; Henk M. Buck 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 228 KB

## 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