Tetrahedron letters

Sonogashira cross-coupling reactions with heteroaryl halides in the presence of a tetraphosphine–palladium catalyst

M Feuerstein, H Doucet, M Santelli

Index: Feuerstein, Marie; Doucet, Henri; Santelli, Maurice Tetrahedron Letters, 2005 , vol. 46, # 10 p. 1717 - 1720

Full Text: HTML

Citation Number: 58

Abstract

Heteroaryl halides undergoes cross-couplings with alkynes in good yields in the presence of [PdCl (C3H5)] 2/cis, cis, cis-1, 2, 3, 4-tetrakis (diphenylphosphinomethyl) cyclopentane as catalyst. A variety of heteroaryl halides such as pyridines, quinolines, a pyrimidine, an indole, a thiophene, or a thiazole have been used successfully. The reaction also tolerates several alkynes such as phenylacetylene and a range of alk-1-ynols. Furthermore, this ...

Related Articles:

Photochemical synthesis and properties of axially chiral naphthylpyridines

[Wessig, Pablo; Pick, Charlotte Journal of Photochemistry and Photobiology A: Chemistry, 2011 , vol. 222, # 1 p. 263 - 265]

Microwave??Enhanced Rhodium??Catalyzed [2+ 2+ 2] Cycloaddition Reactions To Afford Highly Functionalized Pyridines and Bipyridines

[Garcia, Lidia; Pla-Quintana, Anna; Roglans, Anna; Parella, Teodor European Journal of Organic Chemistry, 2010 , # 18 p. 3407 - 3415]

More Articles...