Suzuki-Miyaura reactions of arenediazonium salts catalyzed by Pd (0)/C. One-pot chemoselective double cross-coupling reactions
RH Taylor, FX Felpin
Index: Taylor, Rachel H.; Felpin, Francois-Xavier Organic Letters, 2007 , vol. 9, # 15 p. 2911 - 2914
Full Text: HTML
Citation Number: 90
Abstract
The Suzuki-Miyaura cross-coupling of arenediazonium tetrafluoroborate salts with boronic acid partners catalyzed by Pd (0)/C is described as a practical and efficient alternative to classical homogeneous conditions. Reactions conducted in alcoholic solvents proved to be extremely fast using mild conditions. Additionnaly, we developed a chemoselective double Suzuki-Miyaura cross-coupling in a single reaction vessel allowing the synthesis of ...
Related Articles:
[Zhao, Hong; Peng, Jian; Xiao, Ruian; Cai, Mingzhong Journal of Molecular Catalysis A: Chemical, 2011 , vol. 337, # 1-2 p. 56 - 60]
[Ho, Jinn-Hsuan; Lin, Yu-Chen; Chou, Li-Ting; Chen, Ying-Zhe; Liu, Wei-Qi; Chuang, Chao-Li Tetrahedron Letters, 2013 , vol. 54, # 15 p. 1991 - 1993]
[Ho, Jinn-Hsuan; Lin, Yu-Chen; Chou, Li-Ting; Chen, Ying-Zhe; Liu, Wei-Qi; Chuang, Chao-Li Tetrahedron Letters, 2013 , vol. 54, # 15 p. 1991 - 1993]
[Ho, Jinn-Hsuan; Lin, Yu-Chen; Chou, Li-Ting; Chen, Ying-Zhe; Liu, Wei-Qi; Chuang, Chao-Li Tetrahedron Letters, 2013 , vol. 54, # 15 p. 1991 - 1993]