Copper-catalyzed reaction of aryl iodides with active methylene compounds

…, M Furuune, M Miura, M Nomura

Index: Okuro, Kazumi; Furuune, Makoto; Miura, Masahiro; Nomura, Masakatsu Journal of Organic Chemistry, 1993 , vol. 58, # 26 p. 7606 - 7607

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Citation Number: 124

Abstract

Reaction of aryl halides with carbon nucleophiles such as anions of active methylene compounds promoted by copper species, forming a carbon-carbon bond, is a useful tool for preparation of substituted aromatic compounds. l The reaction usually requires a stoichiometric amount of copper (1) salt, unless the halides are activated by an o- carboxylate gr0up. l On the other hand, we have recently reported that reaction of aryl and ...