P. M. VAN LIER

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

Stereoselective hydride uptake in modelsystems related to the redox-couple nad+/nadh

P.M.T. de Kok, M.C.A. Donkersloot, P. M. VAN LIER et al. · Tetrahedron · 1986 · 39 citations

Biochemistry, Bioenergetics, Natural Sciences +8

A model study of the role of the CONH₂‐group in the redox Co‐enzyme NAD(P)⁺‐NAD(P)H

P. M. VAN LIER, M.C.A. Donkersloot, A. S. Koster et al. · Recueil des Travaux Chimiques des Pays-Bas · 1982 · 17 citations

Stereospecific Incorporation, Model Study, Biochemistry +15

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

H. J. G. van Hooff, P. M. VAN LIER, L. A. M. BASTIAANSEN et al. · Recueil des Travaux Chimiques des Pays-Bas · 1982 · 13 citations

4,5,6,7-Tetrahydrobenzo[b]thiophenes via diisobutylaluminum hydride mediated detosylation reactions

C. G. M. JANSSEN, P. M. VAN LIER, Pieter E. Schipper et al. · The Journal of Organic Chemistry · 1980 · 11 citations

Derivative (Chemistry), Molecular Sciences, Diisobutylaluminum Hydride +11