ChemInform Abstract: The First Heterogeneous Carbonylative Stille Coupling of Organostannanes with Aryl Iodides Catalyzed by MCM-41-Supported Bidentate Phosphine Palladium(0) Complex.

ChemInform ◽  
2010 ◽  
Vol 41 (9) ◽  
Author(s):  
Mingzhong Cai ◽  
Guomin Zheng ◽  
Guodong Ding
Keyword(s):  
Stille Coupling ◽  
Aryl Iodides ◽  
Bidentate Phosphine ◽  
Mcm 41

Synthesis of terminal arylacetylenes by a Stille coupling reaction catalysed by a MCM-41-supported bidentate phosphine palladium(O) complex

2008 ◽  
Vol 2008 (11) ◽  
pp. 615-618 ◽  
Author(s):  
Wenyan Hao ◽  
Yue Wang ◽  
Shouri Sheng ◽  
Mingzhong Cai
Keyword(s):  
Aqueous Medium ◽  
Palladium Catalyst ◽  
Basic Problem ◽  
Coupling Reaction ◽  
Aryl Halides ◽  
Stille Coupling ◽  
Bidentate Phosphine ◽  
Stille Coupling Reaction ◽  
High Yields ◽  
Mcm 41

A variety of terminal arylacetylenes have been conveniently synthesised in good to high yields by Stille coupling of aryl halides with ethynyltributylstannane catalysed by a MCM-41-supported bidentate phosphine palladium(O) complex in an aqueous medium and under air. Our system not only avoids the requirement for water-free and oxygen-free conditions, but also solves the basic problem of palladium catalyst reuse.

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