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Synthesis of indolocarbazole quinones; potent aryl hydrocarbon receptor ligands
Södertörn University, Avdelning Naturvetenskap. Karolinska Institute.
Södertörn University, Avdelning Naturvetenskap. Karolinska Institute.
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2002 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 58, no 7, 1443-1452 p.Article in journal (Refereed) Published
Abstract [en]

Syntheses of indolo[2,3-b]carbazole-6,12-dione and the isomeric indolo[3,2-b]carbazole-6,12-dione, an extremely efficient inducer of the aryl hydrocarbon (Ah) receptor are described. Initial oxidation of the parent indolo[3,2-b]carbazole followed by several different ring-closing strategies produced the latter compound. Entries into syntheses of unsymmetrical 6,12-disubstituted indolo[2,3-b]carbazoles are also described.

Place, publisher, year, edition, pages
2002. Vol. 58, no 7, 1443-1452 p.
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Chemical Sciences
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URN: urn:nbn:se:sh:diva-15816DOI: 10.1016/S0040-4020(02)00006-6ISI: 000174339600023ScopusID: 2-s2.0-0037060086OAI: oai:DiVA.org:sh-15816DiVA: diva2:508332
Available from: 2012-03-08 Created: 2012-03-07 Last updated: 2014-04-16Bibliographically approved

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Bergman, Jan
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