Title of article :
A simple and efficient copper oxide-catalyzed Barbier–Grignard reaction of unactivated aryl or alkyl bromides with ester
Author/Authors :
Gao، نويسنده , , Fei-Yan Deng، نويسنده , , Xiang-Jun and Tang، نويسنده , , Yu and Tang، نويسنده , , Jin-Peng and Yang، نويسنده , , Jun and Zhang، نويسنده , , Yuan-Ming، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2014
Pages :
4
From page :
880
To page :
883
Abstract :
An efficient one-pot route to synthesize tertiary alcohol compounds using Barbier–Grignard reaction of unactivated alkyl or aryl bromides with ester in THF at 65 °C catalyzed by CuO has been developed and systematically investigated. A wide range of substituted tertiary alcohol compounds were obtained in good to high yields. The reaction is highly chemoselective. The mechanism involving the leaving group of R2O-group is discussed.
Keywords :
Ester , Grignard reagent , tertiary alcohol , Synthesis
Journal title :
Tetrahedron Letters
Serial Year :
2014
Journal title :
Tetrahedron Letters
Record number :
1887962
Link To Document :
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