Title of article :
Nickel-catalyzed cross-coupling reaction of acetylenic sulfones with alkynyl Grignard reagents: a facile method for the preparation of unsymmetrical 1,3-diynes
Author/Authors :
Fang، نويسنده , , Kuang and Xie، نويسنده , , Meihua and Zhang، نويسنده , , Zhannan and Ning، نويسنده , , Peng and Shu، نويسنده , , Guanying، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
3
From page :
3819
To page :
3821
Abstract :
The cross-coupling reaction of acetylenic sulfones with acetylenic Grignard reagents was realized by using Ni(acac)2 as catalyst to afford unsymmetrical 1,3-diynes under mild conditions without homocoupling byproducts. By using this method, 1,4-diaryl-1,3-diynes could be obtained in moderate to good yields (59–83%), whereas, the yields for alkyl substituted 1,3-diynes are lower (30–54%).
Keywords :
Grignard reagent , 1 , cross-coupling reaction , 3-diyne , acetylenic sulfone
Journal title :
Tetrahedron Letters
Serial Year :
2013
Journal title :
Tetrahedron Letters
Record number :
1884959
Link To Document :
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