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January 1, 2005Chemical CommunicationsOpen Access

[Cp*Rh(bpy)(H2O)]2+ as a coenzyme substitute in enzymatic oxidations catalyzed by Baeyer–Villiger monooxygenases

Gonzalo de Gonzalo Gianluca Ottolina Giacomo Carrea Marco W. Fraaije

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Abstract

[Cp*Rh(bpy)(H2O)]2+ was applied as a flavin regenerating reagent in BVMO catalyzed oxidations of organic sulfides to chiral sulfoxides.

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Cite This Study

Gonzalo et al. (2005) studied this question.

synapsesocial.com/papers/6a1bcd16ea84844e355efd55 https://doi.org/10.1039/b504921k

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Reduction of Nicotinamides, Flavins, and Manganese Porphyrins by Formate, Catalyzed by Membrane-Bound Rhodium ComplexesOriginal Research · 1995 · 31 citations
2Regioselective Reduction of NAD+ Models with [Cp*Rh(bpy)H]+: Structure-Activity Relationships and Mechanistic Aspects in the Formation of the 1,4-NADH DerivativesOriginal Research · 1999 · 231 citations
3The First Synthetic Application of a Monooxygenase Employing Indirect Electrochemical NADH RegenerationOriginal Research · 2001 · 173 citations
4Stereospecific Biocatalytic Epoxidation: The First Example of Direct Regeneration of a FAD-Dependent Monooxygenase for CatalysisOriginal Research · 2003 · 172 citations
5Crystal structure of a Baeyer–Villiger monooxygenaseOriginal Research · 2004 · 297 citations

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