Journal of organometallic chemistry

Efficient coupling of heteroaryl halides with arylboronic acids in the presence of a palladium–tetraphosphine catalyst

M Feuerstein, H Doucet, M Santelli

Index: Feuerstein, Marie; Doucet, Henri; Santelli, Maurice Journal of Organometallic Chemistry, 2003 , vol. 687, # 2 p. 327 - 336

Full Text: HTML

Citation Number: 72

Abstract

Cis, cis, cis-1, 2, 3, 4-tetrakis (diphenylphosphinomethyl) cyclopentane:· 1/2 [PdCl (C3H5)] 2 system catalyses the Suzuki cross-coupling of heteroaryl halides with a range of arylboronic acids with very high ratio substrate/catalyst in good yields. Substrates such as pyridines, quinolines, thiophenes, an indole, pyrimidines or a furane have been used successfully.

Related Articles:

Isoquinolinium N-arylimides and acetylenic dipolarophiles; cycloadducts and their rearrangements

[Bast, Klaus; Durst, Tony; Huber, Helmut; Huisgen, Rolf; Lindner, Klaus; Stephenson, David S.; Temme, Robert Tetrahedron, 1998 , vol. 54, # 29 p. 8451 - 8468]

Ionic Liquid Supported Organotin Reagents: Green Tools for Stille Cross??Coupling Reactions with Brominated Substrates

[Louaisil, Nicolas; Pham, Phuoc Dien; Boeda, Fabien; Faye, Djibril; Castanet, Anne-Sophie; Legoupy, Stephanie European Journal of Organic Chemistry, 2011 , # 1 p. 143 - 149]

Synthesis of Trimethylstannyl Arylboronate Compounds by Sandmeyer-Type Transformations and Their Applications in Chemoselective Cross-Coupling Reactions

[Qiu, Di; Jin, Liang; Zheng, Zhitong; Meng, He; Mo, Fanyang; Wang, Xi; Zhang, Yan; Wang, Jianbo Journal of Organic Chemistry, 2013 , vol. 78, # 5 p. 1923 - 1933]

More Articles...