about
Suicide Inhibition of Cytochrome P450 Enzymes by Cyclopropylamines via a Ring-Opening Mechanism: Proton-Coupled Electron Transfer Makes a Difference.Manganese complex-catalyzed oxidation and oxidative kinetic resolution of secondary alcohols by hydrogen peroxide.Mutable Properties of Nonheme Iron(III)-Iodosylarene Complexes Result in the Elusive Multiple-Oxidant Mechanism.Theoretical insights into the reductive metabolism of CCl4 by cytochrome P450 enzymes and the CCl4-dependent suicidal inactivation of P450.Tunneling Effect That Changes the Reaction Pathway from Epoxidation to Hydroxylation in the Oxidation of Cyclohexene by a Compound I Model of Cytochrome P450.Reactivity Patterns of (Protonated) Compound II and Compound I of Cytochrome P450: Which is the Better Oxidant?Detoxification of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) by cytochrome P450 enzymes: A theoretical investigation.Bio-activation of 4-alkyl analogs of 1,4-dihydropyridine mediated by cytochrome P450 enzymes.Quantum Mechanics/Molecular Mechanics Studies on the Relative Reactivities of Compound I and II in Cytochrome P450 EnzymesElectron-Transfer and Redox Reactivity of High-Valent Iron Imido and Oxo Complexes with the Formal Oxidation States of Five and SixSingly Unified Driving Force Dependence of Outer-Sphere Electron-Transfer Pathways of Nonheme Manganese(IV)-Oxo Complexes in the Absence and Presence of Lewis AcidsRegioselective Oxybromination of Benzene and Its Derivatives by Bromide Anion with a Mononuclear Nonheme Mn(IV)-Oxo ComplexHigh-Spin Mn(V)-Oxo Intermediate in Nonheme Manganese Complex-Catalyzed Alkane Hydroxylation Reaction: Experimental and Theoretical ApproachMn(III)-Iodosylarene Porphyrins as an Active Oxidant in Oxidation Reactions: Synthesis, Characterization, and Reactivity StudiesTunneling Controls the Reaction Pathway in the Deformylation of Aldehydes by a Nonheme Iron(III)-Hydroperoxo Complex: Hydrogen Atom Abstraction versus Nucleophilic AdditionA Mn(iv)-peroxo complex in the reactions with proton donors
P50
Q37614575-14BBE80D-9786-493C-8059-69A6D3AF73D9Q45420797-7C7F87B1-F470-4202-8F69-B929D1C8F9AFQ46363578-CC47DEEB-8172-4951-8009-C10A70DA8120Q46846588-40657E0B-6857-4787-842C-01E8A1F7566EQ48044772-7D86A6E0-C9F8-4193-AD86-144DBB4F94A0Q48044973-3998FE59-C0B0-45B6-BFF9-1639BD00B9FCQ51655515-F704A059-E8FB-4817-892F-ED97B6363DF3Q52958170-2F117DCE-B06C-4230-8E7B-6DB7932F451DQ61857632-F448C711-BC59-42C1-8444-591B08DA86A5Q89568729-3CA50F00-60EB-4881-BC65-78E40531493EQ90550849-367737E6-1103-4CCA-8101-744D9F615EB9Q90687654-D0681FC6-C3CB-4D05-8F5A-5A0ADECD57E8Q90764511-32714D94-B8A9-46D5-9782-28F9EDC01AB0Q90772086-95D97FFD-E87A-495F-AB15-DB8C9E4377DBQ91601246-00ECDC9A-B32F-461B-BE29-18909C66B513Q92806210-F960A34E-8A86-463E-AF44-0F7B3D78246B
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Xiao-Xi Li
@ast
Xiao-Xi Li
@en
Xiao-Xi Li
@es
Xiao-Xi Li
@nl
type
label
Xiao-Xi Li
@ast
Xiao-Xi Li
@en
Xiao-Xi Li
@es
Xiao-Xi Li
@nl
prefLabel
Xiao-Xi Li
@ast
Xiao-Xi Li
@en
Xiao-Xi Li
@es
Xiao-Xi Li
@nl
P106
P31
P496
0000-0002-3593-7536