期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 781, 期 -, 页码 6-10出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2015.01.009
关键词
Suzuki-Miyaura reaction; Biaryl; Phenol 2,4,6-Trichloro-1,3,5-triazine; Nickel
资金
- research councils of Shiraz University
- Iran National Elite Foundation
In this study, the direct Nickel-catalyzed SuzukieMiyaura coupling reaction of phenols and arylboronic acids via CeO bond activation using 2,4,6-trichloro-1,3,5-triazine (TCT) is described. Initially, phenols were reacted with TCT to give the corresponding 2,4,6-triaryloxy-1,3,5-triazine (TAT) products. Subsequently, arylboronic acid, base and Ni-catalyst were added to the generated aryl CeO electrophile to obtain the final biaryl product. This study represents a simple and direct method for the synthesis of biaryls from phenolic compounds using sub-stoichiometric amounts of TCT as a cheap and readily available CeO activating reagent. (C) 2015 Elsevier B. V. All rights reserved.
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