Literature DB >> 26910536

Nickel-Catalyzed Negishi Cross-Coupling of Bromodifluoroacetamides.

Atsushi Tarui1, Saori Shinohara1, Kazuyuki Sato1, Masaaki Omote1, Akira Ando1.   

Abstract

A nickel-catalyzed Negishi coupling of bromodifluoroacetamides with arylzinc reagents has been developed. This reaction allows access to difluoromethylated aromatic compounds containing a variety of aryl groups and amide moieties. Furthermore, highly effective transformation of the functionalized difluoromethyl group (-CF2CONR(1)R(2)) was realized via microwave-assisted reduction under mild conditions. The notable features of this strategy are its generality and its use of a low-cost nickel catalyst and ligand; thus, this reaction provides a facile method for applications in drug discovery and development.

Entities:  

Year:  2016        PMID: 26910536     DOI: 10.1021/acs.orglett.6b00232

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


  4 in total

Review 1.  The Fascinating Chemistry of α-Haloamides.

Authors:  Anna Fantinati; Vinicio Zanirato; Paolo Marchetti; Claudio Trapella
Journal:  ChemistryOpen       Date:  2020-01-13       Impact factor: 2.911

2.  Using JPP to Identify Ni Bidentate Phosphine Complexes In Situ.

Authors:  Matthew D Hannigan; Anne J McNeil; Paul M Zimmerman
Journal:  Inorg Chem       Date:  2021-08-18       Impact factor: 5.165

3.  A convenient approach to difluoromethylated all-carbon quaternary centers via Ni(ii)-catalyzed enantioselective Michael addition.

Authors:  Xuan Yu; Hui Bai; Dong Wang; Zhaohai Qin; Jia-Qi Li; Bin Fu
Journal:  RSC Adv       Date:  2018-05-25       Impact factor: 3.361

4.  Highly selective nickel-catalyzed gem-difluoropropargylation of unactivated alkylzinc reagents.

Authors:  Lun An; Chang Xu; Xingang Zhang
Journal:  Nat Commun       Date:  2017-11-13       Impact factor: 14.919

  4 in total

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