Literature DB >> 22928706

Suzuki-Miyaura coupling of aryl iodides, bromides, and chlorides catalyzed by bis(thiazole) pincer palladium complexes.

Qun-Li Luo1, Jian-Ping Tan, Zhi-Fu Li, Wen-Hui Nan, Dong-Rong Xiao.   

Abstract

Bis(thiazole) pincer palladium complexes showed efficient catalytic activity for the Suzuki-Miyaura coupling of aryl halides, allowing the synthesis of biaryls with very high turnover numbers and turnover frequencies. The complexes were successfully applied in the scalable and green synthesis of the key intermediates of bioactive LUF5771 and its analogues.

Entities:  

Year:  2012        PMID: 22928706     DOI: 10.1021/jo3011733

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  A synthetic, catalytic and theoretical investigation of an unsymmetrical SCN pincer palladacycle.

Authors:  Gavin W Roffe; Sarote Boonseng; Christine B Baltus; Simon J Coles; Iain J Day; Rhiannon N Jones; Neil J Press; Mario Ruiz; Graham J Tizzard; Hazel Cox; John Spencer
Journal:  R Soc Open Sci       Date:  2016-04-06       Impact factor: 2.963

2.  [2,6-Bis(5-eth-oxy-1,3-oxazol-2-yl)-4-meth-oxy-phenyl-κ(3) N,C (1),N']bromidopalladium(II).

Authors:  Wen-Hui Nan; Jian-Ping Tan; Qun-Li Luo
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-12-08
  2 in total

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