A practical and general synthesis of unsymmetrical terphenyls

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Abstract

(Chemical Equation Presented) A synthetic procedure was developed that enables sequential chemoselective Suzuki-Miyaura cross-coupling of chlorobromobenzene with arylboronic acids. The first coupling is achieved at room temperature using a ligandless palladium catalyst. The chlorobiaryl product can then be subjected directly to the second coupling, facilitated by the SPhos ligand. Using this methodology, parallel synthesis of 32 unsymmetrical o-, m-, and p-terphenyl compounds was accomplished in good to excellent overall yields. © 2007 American Chemical Society.

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Antelo Miguez, J. M., Adrio, L. A., Sousa-Pedrares, A., Vila, J. M., & Hii, K. K. (2007). A practical and general synthesis of unsymmetrical terphenyls. Journal of Organic Chemistry, 72(20), 7771–7774. https://doi.org/10.1021/jo701308b

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