Highly reactive and stereospecific reaction of quinoline-type NADH model compounds with methyl benzoylformate

Reduction by a model of NAD(P)H. 25. A chiral model which induces high asymmetry

Atsuyoshi Ohno, Masahiko Ikeguchi, Takahide Kimura et al. · Journal of the American Chemical Society · 1979 · 145 citations

Altmetrics, Engineering, High Asymmetry +13

A mechanistic basis for the stereoselectivity of enzymic transfer of hydrogen from nicotinamide cofactors

Krishnan P. Nambiar, Dora M. Stauffer, Peter A. Kolodziej et al. · Journal of the American Chemical Society · 1983 · 112 citations

Bioorganic Chemistry, Engineering, Chemical Analysis +20

Highly reactive and stereoselective (R)- and (S)-3-(N,N-dimethylcarbamoyl)-1,2,4-trimethyl-1,4-dihydropyridines for NADH-NAD+ mimicry

P.M.T. de Kok, Loek A. M. Bastiaansen, P. M. VAN LIER et al. · The Journal of Organic Chemistry · 1989 · 80 citations · Full text

Diversity Oriented Synthesis, Molecular Sciences, Bioorganic Chemistry +13

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

M.C.A. Donkersloot, H. M. BUCK · Journal of the American Chemical Society · 1981 · 74 citations

Nad(P)+-nad(p)h models. 57

Atsuyoshi Ohno, Masanori Kashiwagi, Yuji Ishihara et al. · Tetrahedron · 1986 · 61 citations

Aldo-keto Reductase, Natural Sciences, Proton Transfer +5