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Nickel-catalysed Suzuki–Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids.
- Source :
-
Catalysis Communications . Jan2015, Vol. 58, p154-157. 4p. - Publication Year :
- 2015
-
Abstract
- An efficient strategy for the nickel-catalysed synthesis of biaryls and terphenyls has been developed in environmentally-friendly reaction media. In the presence of β-diketone and PPh 3 ligands, Ni(TFA) 2 acted as an effective catalyst for the Suzuki–Miyaura cross-coupling of aryl halides and arylboronic acids in an ionic liquid solution. Biaryls and terphenyls were obtained in good yields under this catalytic system. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 15667367
- Volume :
- 58
- Database :
- Academic Search Index
- Journal :
- Catalysis Communications
- Publication Type :
- Academic Journal
- Accession number :
- 99066685
- Full Text :
- https://doi.org/10.1016/j.catcom.2014.08.037