Formal Decarbonylation of 1,2-Diketones Enabled by Synergistic Catalysis of Lewis Acid–Base Pairs and Redox Properties in CeO2
Author:
Affiliation:
1. Department of Applied Chemistry, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.4c02493
Reference77 articles.
1. Selective Decarbonylation via Transition-Metal-Catalyzed Carbon–Carbon Bond Cleavage
2. Cross-coupling of aromatic esters and amides
3. Carbon–Carbon Bond Cleavage for Late-Stage Functionalization
4. Nickel-Mediated Decarbonylation of Simple Unstrained Ketones through the Cleavage of Carbon–Carbon Bonds
5. Decarbonylation of Aryl Ketones Mediated by Bulky Cyclopentadienylrhodium Bis(ethylene) Complexes
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