Bioorganometallic Chemistry. 13. Regioselective Reduction of NAD+ Models, 1-Benzylnicotinamde Triflate and β-Nicotinamide Ribose-5‘-methyl Phosphate, with in Situ Generated [Cp*Rh(Bpy)H]+: Structure−Activity Relationships, Kinetics, and Mechanistic Aspects in the Formation of the 1,4-NADH Derivatives-Reference-Cited by-同舟云学术

Bioorganometallic Chemistry. 13. Regioselective Reduction of NAD+ Models, 1-Benzylnicotinamde Triflate and β-Nicotinamide Ribose-5‘-methyl Phosphate, with in Situ Generated [Cp*Rh(Bpy)H]+: Structure−Activity Relationships, Kinetics, and Mechanistic Aspects in the Formation of the 1,4-NADH Derivatives

Published:2001-11-10 Issue:26 Volume:40 Page:6705-6716
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Lo H. Christine¹,Leiva Carmen¹,Buriez Olivier¹,Kerr John B.¹,Olmstead Marilyn M.¹,Fish Richard H.¹

Affiliation:

1. Lawrence Berkeley National Laboratory, 70-108B, University of California, Berkeley, California 94720, and Department of Chemistry, University of California, Davis, California 95616

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic010562z

Reference27 articles.

1. Regeneration of nicotinamide cofactors for use in organic synthesis

2. Enzymes in organic synthesis: oxidoreductions

3. Very efficient reduction of NAD(P)+ with formate catalysed by cationic rhodium complexes

4. Analytical study of a series of substituted (2,2'-bipyridyl)(pentamethylcyclopentadienyl)rhodium and -iridium complexes with regard to their effectiveness as redox catalysts for the indirect electrochemical and chemical reduction of NAD(P)+

5. Hydrogenase Enzyme Reactivity Modeling with a Transition-Metal Dihydrogen Complex

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