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Title: A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses
Authors: Fu, WC 
Zhou, Z 
Kwong, FY 
Issue Date: 1-Feb-2016
Source: Organic chemistry frontiers, 1 Feb. 2016, v. 3, no. 2, p. 273-276
Abstract: A new benzo[c]carbazolyl-based phosphine ligand has been designed and synthesized. This newly developed ligand efficiently facilitates the Pd-catalyzed tetra-ortho-substituted biaryl syntheses via Suzuki-Miyaura cross-coupling. With 1 mol% of the Pd(OAc)2/L6 catalyst, sterically congested biaryls were afforded in good-to-excellent yields. In particular, the mild reaction conditions exhibited good compatibility of heterocycles and functional groups including esters and nitrile. L6 was structurally characterized by X-ray crystallographic analysis.
Publisher: Royal Society of Chemistry
Journal: Organic chemistry frontiers 
ISSN: 2052-4129
DOI: 10.1039/c5qo00400d
Rights: This journal is © the Partner Organisations 2016
The following publication Fu, W. C., Zhou, Z., & Kwong, F. Y. (2016). A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses. Organic Chemistry Frontiers, 3(2), 273–276 is available at https://doi.org/10.1039/C5QO00400D.
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