Exploring (Ph 2 PCH 2 CH 2 ) 2 E Ligand Space (E = O, S, PPh) in Rh I Alkene Complexes as Potential Hydroacylation Catalysts
Author:
Affiliation:
1. Department of Chemistry, Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QR, UK
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.201100958
Reference57 articles.
1. Homogeneous catalysis. Mechanism of catalytic hydroacylation: the conversion of 4-pentenals to cyclopentanones
2. Isolation of a stable acylrhodium(III) hydride intermediate formed during aldehyde decarbonylation. Hydroacylation
3. Transition Metal Catalyzed Alkene and Alkyne Hydroacylation
4. Transition-metal-catalyzed carbon-carbon bond formation via carbon-hydrogen activation. Intermolecular hydroacylation: the addition of aldehydes to alkenes
5. Mechanistic Insights into the Rhodium-Catalyzed Intramolecular Ketone Hydroacylation
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