Fe-Catalyzed Aziridination Is Governed by the Electron Affinity of the Active Imido-Iron Species
- 4 September 2020
- journal article
- research article
- Published by American Chemical Society (ACS) in ACS Catalysis
- Vol. 10 (17), 10010-10020
- https://doi.org/10.1021/acscatal.0c01427
Abstract
No abstract availableKeywords
Funding Information
- Council of Scientific and Industrial Research
- Agence Nationale de la Recherche (ANR-17-EURE-0003)
- Science and Engineering Research Board (CRG/2018/001377, EMR/2015/000164, SRG/2019/000310)
- European Cooperation in Science and Technology (CM1305)
This publication has 73 references indexed in Scilit:
- Half-Sandwich Scorpionates as Nitrene Transfer CatalystsOrganometallics, 2012
- A computational examination on the structure, spin-state energetics and spectroscopic parameters of high-valent FeIVNTs speciesDalton Transactions, 2012
- ME and ME complexes of iron and cobalt that emphasize three-fold symmetry (E=O, N, NR)Coordination Chemistry Reviews, 2011
- Enzymatic functionalization of carbon–hydrogen bondsChemical Society Reviews, 2010
- Electronic Structure and Reactivity of Three-Coordinate Iron ComplexesAccounts of Chemical Research, 2008
- Sustainable Metal Catalysis with Iron: From Rust to a Rising Star?Angewandte Chemie-International Edition, 2008
- Copper−Nitrenoid Formation and Transfer in Catalytic Olefin Aziridination Utilizing Chelating 2-Pyridylsulfonyl MoietiesThe Journal of Organic Chemistry, 2008
- Catalytic C–H functionalization by metal carbenoid and nitrenoid insertionNature, 2008
- Spectroscopic and Quantum Chemical Studies on Low-Spin FeIVO Complexes: Fe−O Bonding and Its Contributions to ReactivityJournal of the American Chemical Society, 2007
- Ruthenium-oxo and -tosylimido porphyrin complexes for epoxidation and aziridination of alkenesPublished by Walter de Gruyter GmbH ,1999