1,4-NADH Biomimetic Co-Factors with Horse Liver Alcohol Dehydrogenase (HLADH), Utilizing [Cp*Rh(bpy)H](OTf) for Co-factor Regeneration, Do in Fact, Produce Chiral Alcohols from Reactions with Achiral Ketones-Reference-Cited by-同舟云学术

1,4-NADH Biomimetic Co-Factors with Horse Liver Alcohol Dehydrogenase (HLADH), Utilizing [Cp*Rh(bpy)H](OTf) for Co-factor Regeneration, Do in Fact, Produce Chiral Alcohols from Reactions with Achiral Ketones

Published:2019-06-24 Issue:6 Volume:9 Page:562
ISSN:2073-4344
Container-title:Catalysts
language:en
Short-container-title:Catalysts

Author:

Fish Richard H.

Abstract

In this Catalysts Comment Article, we will present our latest published results [...]

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis

Link

https://www.mdpi.com/2073-4344/9/6/562/pdf

Reference8 articles.

1. Bioorganometallic Chemistry: Co-factor Regeneration, Enzyme Recognition of Biomimetic 1,4-NADH Analogs, and Organic Synthesis; Tandem Catalyzed Regioselective Formation of N-Substituted-1,4 dihydronicotinamide Derivatives with [Cp*Rh(bpy)H]+, Coupled to Chiral S-Alcohol Formation with HLADH, and Engineered Cytochrome P450s, for Selective C-H Oxidation Reactions;Lo;J. Organometal. Chem.,2017

2. Synthetic Biomimetic Coenzymes and Alcohol Dehydrogenases for Asymmetric Catalysis

3. Aqueous Organometallic Chemistry. 3. Catalytic Hydride Transfer Reactions with Ketones and Aldehydes using [Cp*Rh(bpy)(H2O)](OTf)2 as the Precatalyst and Sodium Formate as the Hydride Source: Kinetic and Activation Parameters, and the Significance of Steric and Electronic Effects;Leiva;J. Organometal. Chem.,2010

4. Bioorganometallic Chemistry. 13. Regioselective Reduction of NAD+ Models, N-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;Lo;Inorg. Chem.,2001

5. Biomimetic NAD+ Models for Tandem Cofactor Regeneration, Horse Liver Alcohol Dehydrogenase Recognition of 1,4-NADH Derivatives, and Chiral Synthesis

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1. A computational insight on the aromatic amino acids conjugation with [Cp*Rh(H2O)3]2+ by using the meta-dynamics/FMO3 approach;Journal of Molecular Modeling;2023-12-12

2. Bioorganometallic Chemistry at the Interface with Biocatalysis: Chemoselective Reduction of Biomimetic NAD⁺ Cofactors with [Cp*Rh(bpy)H]⁺, Tandem Catalysis with 1,4-NADH-Dependent Enzymes, Chiral Synthesis, Organotin Metabolites, and DFT Mechanism Studies;Organometallics;2023-02-07

3. MD-DFT Computational Studies on the Mechanistic and Conformational Parameters for the Chemoselective Tyrosine Residue Reactions of G-Protein-Coupled Receptor Peptides with [Cp*Rh(H₂O)₃](OTf)₂ in Water To Form Their [(η⁶-Cp*Rh-Tyr^#)-GPCR peptide]²⁺ Complexes: Noncovalent H-Bonding Interactions, Molecular Orbital Analysis, Thermodynamics, and Lowest Energy Conformations;Organometallics;2022-08-11

4. A Tailor-Made Deazaflavin-Mediated Recycling System for Artificial Nicotinamide Cofactor Biomimetics;ACS Catalysis;2021-09-02

5. DFT Mechanism Studies: Biomimetic 1,4-NADH Chemoselective, Co-factor Regeneration with [Cp*Rh(bpy)H]+, in Tandem with the Biocatalysis Pathways of a Core Model of the (HLADH)-Zn(II) Mediated Enzyme, in the Enantioselective Reduction of Achiral Ketones to Chiral S-Alcohols;Journal of Organometallic Chemistry;2021-06