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http://dx.doi.org/10.5012/bkcs.2004.25.12.1924

Zinc Mediated Barbier Type Allylation of Cyclic Imides and Subsequent Coupling Reactions with Carbon Nucleophiles  

Kang, Seok-Won (Department of Chemistry, Konkuk University)
Heo, Eun-Young (Department of Chemistry, Konkuk University)
Jun, Jong-Gab (Department of Chemistry, Hallym University)
Kim, Sung-Hoon (Department of Chemistry, Konkuk University)
Publication Information
Bulletin of the Korean Chemical Society / v.25, no.12, 2004 , pp. 1924-1928 More about this Journal
Abstract
Allylations of N-benzyl and N-methyl cyclic imides were accomplished successfully under mild Barbier type conditions using zinc metal, allyl bromide and catalytic amount of $PbBr_2$. Subsequent coupling reactions with some carbon nucleophiles afforded 1,2- and 1,4-addition products in moderate to high yields.
Keywords
Allylation; Cyclic imide; Barbier; N-Acyliminium ion; Carbon nucleophiles;
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Times Cited By Web Of Science : 6  (Related Records In Web of Science)
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