3H??indolium salts efficiently prepared from N??substituted anilines and α??branched ketones by an one??pot synthesis
T Zimmermann, O Brede
Index: Zimmermann, Thomas; Brede, Ortwin Journal of Heterocyclic Chemistry, 2004 , vol. 41, # 1 p. 103 - 108
Full Text: HTML
Citation Number: 6
Abstract
Abstract Starting with the N-substituted anilines 4/12 and the α-branched ketones 3 the 3H- indolium salts 1 and their fused derivatives 13 are prepared by combining a sodium nitrite nitrosation, a zinc dust reduction, a hydrazone formation and a Fischer indolization to a reaction sequence in which the isolation and purification of intermediates is not necessary. The scope and limitations of this effective one-pot synthesis are discussed.
Related Articles:
[Kiyose, Kazuki; Hanaoka, Kenjiro; Oushiki, Daihi; Nakamura, Tomomi; Kajimura, Mayumi; Suematsu, Makoto; Nishimatsu, Hiroaki; Yamane, Takehiro; Terai, Takuya; Hirata, Yasunobu; Nagano, Tetsuo Journal of the American Chemical Society, 2010 , vol. 132, # 45 p. 15846 - 15848]
[Bioorganic and Medicinal Chemistry Letters, , vol. 22, # 24 p. 7667 - 7671]
[Bioorganic and Medicinal Chemistry Letters, , vol. 22, # 24 p. 7667 - 7671]
[Research on Chemical Intermediates, , vol. 39, # 8 p. 3525 - 3530]