» Articles » PMID: 23609983

Catalytic Phenol Hydroxylation with Dioxygen: Extension of the Tyrosinase Mechanism Beyond the Protein Matrix

Overview
Specialty Chemistry
Date 2013 Apr 24
PMID 23609983
Citations 19
Authors
Affiliations
Soon will be listed here.
Citing Articles

Dioxygenase Chemistry in Nucleophilic Aldehyde Deformylations Utilizing Dicopper O-Derived Peroxide Complexes.

Hota P, Panda S, Phan H, Kim B, Siegler M, Karlin K J Am Chem Soc. 2024; 146(34):23854-23871.

PMID: 39141923 PMC: 11472664. DOI: 10.1021/jacs.4c06243.


Experimental Evidence and Mechanistic Description of the Phenolic H-Transfer to the CuO Active Site of oxy-Tyrosinase.

Kipouros I, Stanczak A, Dunietz E, Ginsbach J, Srnec M, Rulisek L J Am Chem Soc. 2023; 145(42):22866-22870.

PMID: 37844210 PMC: 10615789. DOI: 10.1021/jacs.3c07450.


Electrooxidation of Phenol on Polyelectrolyte Modified Carbon Electrodes for Use in Insulin Pump Infusion Sets.

Zhou L, Huber D, van Antwerp B, Pennathur S J Diabetes Sci Technol. 2022; 18(3):625-634.

PMID: 36112811 PMC: 11089874. DOI: 10.1177/19322968221123083.


Copper-Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism.

Schneider R, Engesser T, Nather C, Krossing I, Tuczek F Angew Chem Int Ed Engl. 2022; 61(25):e202202562.

PMID: 35344617 PMC: 9323449. DOI: 10.1002/anie.202202562.


X-ray-Based Techniques to Study the Nano-Bio Interface.

Sanchez-Cano C, Alvarez-Puebla R, Abendroth J, Beck T, Blick R, Cao Y ACS Nano. 2021; 15(3):3754-3807.

PMID: 33650433 PMC: 7992135. DOI: 10.1021/acsnano.0c09563.


References
1.
WESTERFELD W . The inactivation of oestrone. Biochem J. 1940; 34(1):51-8. PMC: 1265245. DOI: 10.1042/bj0340051. View

2.
Palavicini S, Granata A, Monzani E, Casella L . Hydroxylation of phenolic compounds by a peroxodicopper(II) complex: further insight into the mechanism of tyrosinase. J Am Chem Soc. 2005; 127(51):18031-6. DOI: 10.1021/ja0544298. View

3.
Yamazaki S, Itoh S . Kinetic evaluation of phenolase activity of tyrosinase using simplified catalytic reaction system. J Am Chem Soc. 2003; 125(43):13034-5. DOI: 10.1021/ja036425d. View

4.
Kahn V, Ben-Shalom N . N-acetyl-L-tyrosine (NAT) as a substrate for mushroom tyrosinase. Pigment Cell Res. 1998; 11(1):24-33. DOI: 10.1111/j.1600-0749.1998.tb00707.x. View

5.
Mirica L, Ottenwaelder X, Stack T . Structure and spectroscopy of copper-dioxygen complexes. Chem Rev. 2004; 104(2):1013-45. DOI: 10.1021/cr020632z. View