Hydroxylation of an Aliphatic C−H Bond in an Imidazole-Ligated (μ-η2:η2-Peroxo)dicopper(II) Complex
Author:
Affiliation:
1. Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic961187r
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1. Oxygen-18 kinetic isotope effects in the dopamine .beta.-monooxygenase reaction: Evidence for a new chemical mechanism in non-heme, metallomonooxygenase
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3. Copper monooxygenase models: hydroxylation reactions resulting from dioxygen activation by copper(I) complexes
4. Functional Model of Dopamine .beta.-Hydroxylase. Quantitative Ligand Hydroxylation at the Benzylic Position of a Copper Complex by Dioxygen
5. Reaction aspects of a .mu.-peroxo binuclear copper(II) complex
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