Organylzinc Chalcogenolate Promoted Michael‐Type Addition of α,β‐Unsaturated Carbonyl Compounds

作者: Vanessa Lóren Nunes , Ingryd Cristina de Oliveira , Olga Soares do Rêgo Barros

DOI: 10.1002/EJOC.201301497

关键词:

摘要: We present the chemo-, regio-, and stereoselective synthesis of vinyl chalcogenide compounds promoted by organylzinc chalcogenolates. In this protocol, reductive cleavage diorganyl dichalcogenide bonds Zn/NH4OH system led to The reaction was performed with propiolic acids esters afforded β-organochalcogenacrylic under mild basic conditions. stereochemistry corresponded anti-Markovnikov addition organyl chalcogenolate constituents across triple bond.

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