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Synthesis of cyclopent[b]indolones
Department of Organic Chemistry, CNT, Novum Research Park, S-141 52 Huddinge Sweden.
Department of Organic Chemistry, Royal Institute of Technology, 8-100 44 Stockholm Sweden.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
1990 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 46, no 17, 6067-6084 p.Article in journal (Refereed) Published
Abstract [en]

A number of cyclopent[b]indol-1-ones as well as -3-ones have been synthesized, using a new methodology involving intramolecular ring closure of α,β-unsaturated acylindoles. In some cases 1,2,3,4-tetrahydrocarbazol-4-ones were obtained. This methodology was used in the syntheses of the indole alkaloid yuehchukene and the carbazole alkaloid analogue demethoxycarbazomycin B.

Place, publisher, year, edition, pages
1990. Vol. 46, no 17, 6067-6084 p.
National Category
Natural Sciences
URN: urn:nbn:se:uu:diva-140727DOI: 10.1016/S0040-4020(01)87931-XOAI: oai:DiVA.org:uu-140727DiVA: diva2:384264
Available from: 2011-01-08 Created: 2011-01-08 Last updated: 2011-12-02Bibliographically approved

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Gogoll, Adolf
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Organic Chemistry I
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