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.
Original language | English |
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Pages (from-to) | 273-276 |
Number of pages | 4 |
Journal | Organic Chemistry Frontiers |
Volume | 3 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2016 |
ASJC Scopus subject areas
- Organic Chemistry