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http://hdl.handle.net/10397/95269
| 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. |
| Appears in Collections: | Journal/Magazine Article |
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| File | Description | Size | Format | |
|---|---|---|---|---|
| Fu_Benzo-Carbazolyl-Based_Phosphine_Ligand.pdf | Pre-Published version | 703.57 kB | Adobe PDF | View/Open |
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