Literature DB >> 16872196

CoBr2(Bpy): an efficient catalyst for the direct conjugate addition of aryl halides or triflates onto activated olefins.

Muriel Amatore1, Corinne Gosmini, Jacques Périchon.   

Abstract

An efficient cobalt-catalyzed method devoted to the direct conjugate addition of functionalized aryl compounds onto Michael acceptors is described. The CoBr2(2,2'-bipyridine) complex appears to be an extremely suitable catalyst for the activation of a variety of aromatic reagents ranging from halides to triflates functionalized by reactive groups. This procedure allows for the synthesis of compounds resulting from 1,4-addition in good to excellent yields. The versatility of this original process represents a simple alternative to most known methods using organometallic reagents.

Entities:  

Year:  2006        PMID: 16872196     DOI: 10.1021/jo060855f

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


  3 in total

1.  Nickel-catalyzed reductive conjugate addition to enones via allylnickel intermediates.

Authors:  Ruja Shrestha; Stephanie C M Dorn; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2013-01-08       Impact factor: 15.419

2.  Triphenylphosphine Dibromide: A Simple One-pot Esterification Reagent.

Authors:  Christophe Salomé; Harold Kohn
Journal:  Tetrahedron       Date:  2009-01-10       Impact factor: 2.457

3.  Cobalt Catalyzed C-P Bond Formation by Cross-Coupling of Boronic Acids with P(O)H Compounds in Presence of Zinc.

Authors:  Ian Hicks; Jonathan McTague; Tatiana Hapatsha; Rania Teriak; Parminder Kaur
Journal:  Molecules       Date:  2020-01-10       Impact factor: 4.411

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.