Copper(I)/Dioxygen Reactivity with Dinuclear Compounds: Catalytic Oxygenation and Oxo-Transfer to a Ketone
Author:
Affiliation:
1. Department of Chemistry, The Johns Hopkins University, Charles & 34th Streets, Baltimore, Maryland 21218
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic951490c
Reference24 articles.
1. For reviews see, (a) Kitajima, N.; Moro-oka, Y.Chem. Rev.1994,94, 737−757. (b) Fox, S.; Karlin, K. D. InActive Oxygen in Biochemistry; Valentine, J. S., Foote, C. S., Greenberg, A., Liebman, J. F., Eds.; Blackie Academic & Professional, Chapman & Hall: Glasgow, Scotland, 1995; pp 188−231. (c) Karlin, K. D.; Tyeklár, Z. InAdvances in Inorganic Biochemistry; Eichhorn, G. L., Marzilli, L. G., Eds.; Prentice Hall: Englewood Cliffs, NJ, 1994; Vol. 9; pp 123−172.
2. Direct Conversion of Phenols to o-Quinones by Copper(I) Dioxygen. Questions Regarding the Monophenolase Activity of Tyrosinase Mimics
3. Dioxygen-copper reactivity and functional modeling of hemocyanins. Reversible binding of O2 and carbon monoxide to dicopper(I) complexes [CuI2(L)]2+ (L = dinucleating ligand) and the structure of a bis(carbonyl) adduct, [CuI2(L)(CO)2]2+
4. A Model of Internal Monooxygenase Catalyzed Reactions: Copper-Catalyzed Autoxidation of Bis(1-methylbenzimidazol-2-yl)methane
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