N−H versus C−H Activation of a Pyrrole Imine at {Cp*Ir}: A Computational and Experimental Study-Reference-Cited by-同舟云学术

N−H versus C−H Activation of a Pyrrole Imine at {Cp*Ir}: A Computational and Experimental Study

Published:2006-11-23 Issue:26 Volume:25 Page:5976-5978
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Davies David L.¹,Donald Steven M. A.¹,Al-Duaij Omar¹,Fawcett John¹,Little Craig¹,Macgregor Stuart A.¹

Affiliation:

1. Department of Chemistry, University of Leicester, Leicester LE1 7RH, U.K., and School of Engineering and Physical Sciences, William Perkin Building, Heriot-Watt University, Edinburgh EH14 4AS, U.K.

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om060863m

Reference19 articles.

1. Room-temperature cyclometallation of amines, imines and oxazolines with [MCl2Cp*]2(M = Rh, Ir) and [RuCl2(p-cymene)]2

2. Computational Study of the Mechanism of Cyclometalation by Palladium Acetate

3. Electrophilic C−H Activation at {Cp*Ir}: Ancillary-Ligand Control of the Mechanism of C−H Activation

4. Theoretical Studies of the Mechanism of Aerobic Alcohol Oxidation with Palladium Catalyst Systems

5. Mechanistic Characterization of Aerobic Alcohol Oxidation Catalyzed by Pd(OAc)2/Pyridine Including Identification of the Catalyst Resting State and the Origin of Nonlinear [Catalyst] Dependence

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