Abstract
Palladium-catalyzed tandem reactions of 2-alkenylphenyl-acetylenes with CuCl2 or CuBr2 afforded 3-chloro- or 3-bromo-1-methyleneindenes in good yields; these compounds could be further elaborated viapalladium-catalyzed coupling reactions.
* Corresponding authors
a
Department of Chemistry, Fudan University, 220 Handan Road, China
E-mail:
jie_wu@fudan.edu.cn
Fax: +86 21 6510 2412
Tel: +86 21 5566 4619
b Laboratory of Advanced Materials, Fudan University, 220 Handan Road, China
c State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, China
Palladium-catalyzed tandem reactions of 2-alkenylphenyl-acetylenes with CuCl2 or CuBr2 afforded 3-chloro- or 3-bromo-1-methyleneindenes in good yields; these compounds could be further elaborated viapalladium-catalyzed coupling reactions.
S. Ye, K. Gao, H. Zhou, X. Yang and J. Wu, Chem. Commun., 2009, 5406 DOI: 10.1039/B909178E
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