Hydroxylation of Aromatics by H 2 O 2 Catalyzed by Mononuclear Non‐heme Iron Complexes: Role of Triazole Hemilability in Substrate‐Induced Bifurcation of the H 2 O 2 Activation Mechanism-Reference-Cited by-同舟云学术

Hydroxylation of Aromatics by H 2 O 2 Catalyzed by Mononuclear Non‐heme Iron Complexes: Role of Triazole Hemilability in Substrate‐Induced Bifurcation of the H 2 O 2 Activation Mechanism

Published:2019-12-16 Issue:3 Volume:26 Page:659-668
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Rebilly Jean‐Noël¹^ORCID,Zhang Wenli¹,Herrero Christian¹,Dridi Hachem¹,Sénéchal‐David Katell¹,Guillot Régis¹,Banse Frédéric¹^ORCID

Affiliation:

1. Institut de Chimie Moléculaire et des Matériaux d'OrsayUniversité Paris-Sud, Université Paris-Saclay 91405 Orsay cedex France

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201903239

Reference59 articles.

1. Handbook on Metalloproteins

2. Dioxygen Activation at Mononuclear Nonheme Iron Active Sites: Enzymes, Models, and Intermediates

3. Diverse reactions catalyzed by naphthalene dioxygenase fromPseudomonas sp strain NCIB 9816

4. Substrate binding site of naphthalene 1,2-dioxygenase: functional implications of indole binding 1 1Edited by D. C. Rees

5. Crystal Structure of Naphthalene Dioxygenase: Side-on Binding of Dioxygen to Iron

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