Literature DB >> 11277799

Convenient and efficient Suzuki-Miyaura cross-coupling catalyzed by a palladium/diazabutadiene system.

G A Grasa1, A C Hillier, S P Nolan.   

Abstract

[structure: see text]. A Pd(OAc)2/diazabutadiene system has been developed for the catalytic cross-coupling of aryl halides with arylboronic acids. A combination of the diazabutadiene DAB-Cy (1, N,N'-dicyclohexyl-1,4-dizabutadiene) and Pd(OAc)2 was found to form an excellent catalyst for the Suzuki-Miyaura cross-coupling of various aryl bromides and activated aryl chlorides with arylboronic acids.

Entities:  

Year:  2001        PMID： 11277799     DOI： 10.1021/ol015676t

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  2 in total

1.  N,N'-[(2E,3E)-Butane-2,3-diylidene]bis[4-fluoro-2-(1-phenyl-eth-yl)aniline].

Authors:  Juanjuan Wei; Houde She; Lijun Shi; Ziqiang Lei
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-02-12

2.  Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides.

Authors:  Yi Lai; Zhijian Zong; Yujie Tang; Weimin Mo; Nan Sun; Baoxiang Hu; Zhenlu Shen; Liqun Jin; Wen-Hua Sun; Xinquan Hu
Journal:  Beilstein J Org Chem       Date:  2017-02-03       Impact factor: 2.883
  2 in total

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