Synlett

Mild, efficient and highly stereoselective synthesis of (Z)-vinyl chalcogenides from vinyl bromides catalyzed by copper (I) in ionic liquids based on amino acids

Z Wang, H Mo, W Bao

Index: Wang, Zhiming; Mo, Hanjie; Bao, Weiliang Synlett, 2007 , # 1 p. 91 - 94

Full Text: HTML

Citation Number: 31

Abstract

Abstract A method for the synthesis of (Z)-vinyl chalcogenides by the coupling of vinyl bromides with thiols or diphenyl diselenide using copper (I) salts as catalysts in ionic liquids based on amino acids is reported. The desired vinyl chalcogenides were obtained in good to excellent yields with retention of stereochemistry. The ionic liquids play multiple roles in the reaction: they act as solvent, base, and excellent promoter for the copper-catalyzed ...

Related Articles:

Stereospecific synthesis of alkenyl sulphides by cross-coupling reactions of secondary alkyl Grignard reagents with Z-or E-1-bromo-2-phenylthioethene in the …

[Fiandanese, Vito; Miccoli, Giovanni; Naso, Francesco; Ronzini, Ludovico Journal of Organometallic Chemistry, 1986 , vol. 312, p. 343 - 348]

More Articles...