C–H bond activation by high-valent iron/cobalt–oxo complexes: a quantum chemical modeling approach-Reference-Cited by-同舟云学术

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C–H bond activation by high-valent iron/cobalt–oxo complexes: a quantum chemical modeling approach

Published:2024 Issue:5 Volume:26 Page:4349-4362
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Kumar Manjeet¹^ORCID,Gupta Manoj Kumar¹^ORCID,Ansari Mursaleem²,Ansari Azaj¹^ORCID

Affiliation:

1. Department of Chemistry, Central University of Haryana, Mahendergarh-123031, Haryana, India

2. Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, Germany

Abstract

The steric and electronic effect can control the reactivity during C–H bond activation of organic compounds by high-valent metal-oxo species.

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CP/D3CP05866B

Reference134 articles.

1. Adding Aliphatic C–H Bond Oxidations to Synthesis

2. Recent advances in transition metal-catalyzed olefinic C–H functionalization

3. C–H Activation: Toward Sustainability and Applications

4. Rhodium-Promoted C–H Bond Activation of Quinoline, Methylquinolines, and Related Mono-Substituted Quinolines

5. Palladium-Catalyzed Direct C–H Alkenylation with Enol Pivalates Proceeds via Reversible C–O Oxidative Addition to Pd(0)

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