A convenient synthesis of 2-substituted indoles by the reaction of 2-(chloromethyl) phenyl isocyanides with organolithiums
K Kobayashi, D Iitsuka, S Fukamachi, H Konishi
Index: Kobayashi, Kazuhiro; Iitsuka, Daisuke; Fukamachi, Shuhei; Konishi, Hisatoshi Tetrahedron, 2009 , vol. 65, # 36 p. 7523 - 7526
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Citation Number: 16
Abstract
The reaction of 2-(chloromethyl) phenyl isocyanides, readily available by dehydration of the respective N-[2-(chloromethyl) phenyl] formamides, with organolithiums produced 2- substituted indoles in satisfactory yields through addition of organolithiums to the isocyano carbon followed by intramolecular substitution reaction of the resulting imidoyl anion intermediates.
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