Synthesis of cyclopent[b]indolones
1990 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 46, no 17, 6067-6084 p.Article in journal (Refereed) Published
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.
IdentifiersURN: urn:nbn:se:uu:diva-140727DOI: 10.1016/S0040-4020(01)87931-XOAI: oai:DiVA.org:uu-140727DiVA: diva2:384264