Format

Send to

Choose Destination
J Org Chem. 2016 May 20;81(10):4244-51. doi: 10.1021/acs.joc.6b00570. Epub 2016 May 10.

Phosphine-Free, Heterogeneous Palladium-Catalyzed Atom-Efficient Carbonylative Cross-Coupling of Triarylbismuths with Aryl Iodides: Synthesis of Biaryl Ketones.

Author information

1
Key Laboratory of Functional Small Organic Molecule, Ministry of Education and College of Chemistry & Chemical Engineering, Jiangxi Normal University , Nanchang 330022, P. R. China.

Abstract

A novel and highly efficient heterogeneous palladium-catalyzed carbonylative cross-coupling of aryl iodides with triarylbismuths has been developed that proceeds smoothly at atmospheric CO pressure and provides a general and powerful tool for the preparation of various valuable biaryl ketones with high atom economy, good to excellent yield, and recyclability of the catalyst. The reaction is the first example of Pd-catalyzed carbonylative cross-coupling for the construction of biaryl ketones using triarylbismuths as substrates.

PMID:
27129099
DOI:
10.1021/acs.joc.6b00570

Supplemental Content

Full text links

Icon for American Chemical Society
Loading ...
Support Center