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DOI: 10.1039/A807895E (Paper) Reference Section for: J. Chem. Soc., Perkin Trans. 1, 1999, 327-334

Michael additions of 1,2-dihydro-3H-indol-3-ones and some reactions of Michael adducts with ammonium acetate

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Tomomi Kawasaki, Chen-Ying Tang, Hiroyuki Nakanishi, Shuiti Hirai, Tomohisa Ohshita, Mami Tanizawa, Motomu Himori, Hiroshi Satoh, Masanori Sakamoto, Keiko Miura and Fumio Nakano

Abstract

Reactions of 1-acetyl-1,2-dihydro-3H-indol-3-one and 1-acetyl-2-methoxy-1,2-dihydro-3H-indol-3-one with ethylenic and acetylenic carbonyl compounds took place with Michael addition to give 1,3-di- and/or 1,2,3-tri-acylpropane compounds, respectively, which were elaborated to provide several kinds of heterocyclic compounds: carbazoles, oxaspiroindoles, a pyrano[3,2-b]indole, pyrroles and pyrrolo[1,2-a]indoles.

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