Related references
Note: Only part of the references are listed.Copper-Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism
Rebecca Schneider et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2022)
Homogeneous oxidative transformations mediated by copper catalyst systems
Lindie Marais et al.
COORDINATION CHEMISTRY REVIEWS (2021)
Immune properties of invertebrate phenoloxidases*
Lage Cerenius et al.
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY (2021)
Exceptional Substrate Diversity in Oxygenation Reactions Catalyzed by a Bis(μ-oxo) Copper Complex
Melanie Paul et al.
CHEMISTRY-A EUROPEAN JOURNAL (2020)
The ORCA quantum chemistry program package
Frank Neese et al.
JOURNAL OF CHEMICAL PHYSICS (2020)
Copper-Promoted Functionalization of Organic Molecules: from Biologically Relevant Cu/O2 Model Systems to Organometallic Transformations
Rachel Trammell et al.
CHEMICAL REVIEWS (2019)
Employing Linear Tridentate Ligands with Pyrazole End Groups in Catalytic Tyrosinase Model Chemistry: Does Hemilability Matter?
Benjamin Herzigkeit et al.
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY (2019)
A Stereoselective Tyrosinase Model Compound Derived from an m-Xylyl-L-histidine Ligand
Eliana Lo Presti et al.
INORGANIC CHEMISTRY (2019)
Software update: the ORCA program system, version 4.0
Frank Neese
WILEY INTERDISCIPLINARY REVIEWS-COMPUTATIONAL MOLECULAR SCIENCE (2018)
High-valent copper in biomimetic and biological oxidations
William Keown et al.
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY (2017)
Record Broken: A Copper Peroxide Complex with Enhanced Stability and Faster Hydroxylation Catalysis
Patricia Liebhaeuser et al.
CHEMISTRY-A EUROPEAN JOURNAL (2017)
Activation Mechanism of the Streptomyces Tyrosinase Assisted by the Caddie Protein
Yasuyuki Matoba et al.
BIOCHEMISTRY (2017)
Optimization and biological evaluation of 2-aminobenzothiazole derivatives as Aurora B kinase inhibitors
Eun Lee et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2017)
A dinuclear biomimetic Cu complex derived from L-histidine: synthesis and stereoselective oxidations
Maria L. Perrone et al.
DALTON TRANSACTIONS (2017)
Small-molecule models of tyrosinase: From ligand hydroxylation to catalytic monooxygenation of external substrates
Jessica Nadine Hamann et al.
COORDINATION CHEMISTRY REVIEWS (2017)
Copper-Oxygen Complexes Revisited: Structures, Spectroscopy, and Reactivity
Courtney E. Elwell et al.
CHEMICAL REVIEWS (2017)
Structural and Reactivity Models for Copper Oxygenases: Cooperative Effects and Novel Reactivities
Joan Serrano-Plana et al.
ACCOUNTS OF CHEMICAL RESEARCH (2015)
Catalytic aerobic oxidation of phenols to ortho-quinones with air-stable copper precatalysts
M. S. Askari et al.
DALTON TRANSACTIONS (2015)
Catalytic Models of Tyrosinase: Reactivity Differences between Systems Based on Mono- and Binucleating Ligands
Julia Schottenheim et al.
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY (2015)
A Biomimetic Mechanism for the Copper-Catalyzed Aerobic Oxygenation of 4-tert-Butylphenol
Mohammad S. Askari et al.
INORGANIC CHEMISTRY (2015)
Catalytic oxygenation of various monophenols by copper(I) complexes with bis(pyrazolyl)methane ligands: differences in reactivity
Jessica Nadine Hamann et al.
JOURNAL OF COORDINATION CHEMISTRY (2015)
The dark side of sunlight and melanoma
John-Stephen Taylor
SCIENCE (2015)
SHELXT - Integrated space-group and crystal-structure determination
George M. Sheldrick
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES (2015)
Crystal structure refinement with SHELXL
George M. Sheldrick
ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY (2015)
New catalytic model systems of tyrosinase: fine tuning of the reactivity with pyrazole-based N-donor ligands
Jessica Nadine Hamann et al.
CHEMICAL COMMUNICATIONS (2014)
Copper Active Sites in Biology
Edward I. Solomon et al.
CHEMICAL REVIEWS (2014)
Diverse immune functions of hemocyanins
Christopher J. Coates et al.
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY (2014)
Controlling the Catalytic Aerobic Oxidation of Phenols
Kenneth Virgel N. Esguerra et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)
Catalytic Conversion of Monophenols to Ortho-Quinones in a Tyrosinase-Like Fashion: Towards More Biomimetic and More Efficient Model Systems
Julia Schottenheim et al.
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE (2013)
The ORCA program system
Frank Neese
WILEY INTERDISCIPLINARY REVIEWS-COMPUTATIONAL MOLECULAR SCIENCE (2012)
Copper-O-2 reactivity of tyrosinase models towards external monophenolic substrates: molecular mechanism and comparison with the enzyme
Malte Rolff et al.
CHEMICAL SOCIETY REVIEWS (2011)
Copper dioxygen (bio) inorganic chemistry
Edward I. Solomon et al.
FARADAY DISCUSSIONS (2011)
Reactions of Copper(II)-Phenol Systems with O2: Models for TPQ Biosynthesis in Copper Amine Oxidases
Kae Tabuchi et al.
INORGANIC CHEMISTRY (2011)
Effect of the Damping Function in Dispersion Corrected Density Functional Theory
Stefan Grimme et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2011)
The First Catalytic Tyrosinase Model System Based on a Mononuclear Copper(I) Complex: Kinetics and Mechanism
Matte Rolff et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2010)
O-2 Activation and Selective Phenolate ortho Hydroxylation by an Unsymmetric Dicopper mu-eta(1):eta(1)-Peroxido Complex
Isaac Garcia-Bosch et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2010)
A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu
Stefan Grimme et al.
JOURNAL OF CHEMICAL PHYSICS (2010)
Efficient, approximate and parallel Hartree-Fock and hybrid DFT calculations. A 'chain-of-spheres' algorithm for the Hartree-Fock exchange
Frank Neese et al.
CHEMICAL PHYSICS (2009)
Cu[Al(ORF)(4)] Starting Materials and their Application in the Preparation of [Cu(S-n)](+) (n=12, 8) Complexes
Gustavo Santiso-Quinones et al.
CHEMISTRY-A EUROPEAN JOURNAL (2009)
Aromatic Hydroxylation in a Copper Bis(imine) Complex Mediated by a mu-eta(2):eta(2) Peroxo Dicopper Core: A Mechanistic Scenario
Ole Sander et al.
CHEMISTRY-A EUROPEAN JOURNAL (2008)
Modeling tyrosinase activity. Effect of ligand topology on aromatic ring hydroxylation: An overview
Anindita De et al.
JOURNAL OF INORGANIC BIOCHEMISTRY (2008)
Quantum Chemical Approach to the Mechanism for the Biological Conversion of Tyrosine to Dopaquinone
Toshinori Inoue et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2008)
Chemistry with weakly-coordinating fluorinated alkoxyaluminate anions: Gas phase cations in condensed phases?
Ingo Krossing et al.
COORDINATION CHEMISTRY REVIEWS (2006)
Selective DNA strand scission with binuclear copper complexes:: Implications for an active Cu2-O2 species
Sunita Thyagarajan et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2006)
Crystallographic evidence that the dinuclear copper center of tyrosinase is flexible during catalysis
Y Matoba et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Accurate Coulomb-fitting basis sets for H to Rn
F Weigend
PHYSICAL CHEMISTRY CHEMICAL PHYSICS (2006)
The first crystal structure of tyrosinase: All questions answered?
Heinz Decker et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2006)
Influence of ligand rigidity and ring substitution on the structural and electronic behavior of trivalent iron and gallium complexes with asymmetric tridentate ligands
C Imbert et al.
INORGANIC CHEMISTRY (2005)
Tuning of copper(I)-dioxygen reactivity by bis(guanidine) ligands
S Herres-Pawlis et al.
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY (2005)
Tyrosinase reactivity in a model complex: An alternative hydroxylation mechanism
LM Mirica et al.
SCIENCE (2005)
Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy
F Weigend et al.
PHYSICAL CHEMISTRY CHEMICAL PHYSICS (2005)
Structure and spectroscopy of copper-dioxygen complexes
LM Mirica et al.
CHEMICAL REVIEWS (2004)
Reaction behaviour of dinuclear copper(I) complexes with m-xylyl-based ligands towards dioxygen
SP Foxon et al.
DALTON TRANSACTIONS (2004)
Ag(P4)2+:: The first homoleptic metal-phosphorus cation
I Krossing
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2001)
Share Paper
