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Synthetic Applications of Cyanoacetylated Bisindoles: Synthesis of Novel Cycloheptadiindoles, Indolocarbazoles, and Related Aza Analogues.
Unit for Organic Chemistry, Department of Biosciences and Nutrition, Karolinska Institute, Novum Research Park.
Unit for Organic Chemistry, Department of Biosciences and Nutrition, Karolinska Institute, Novum Research Park.ORCID iD: 0000-0002-8444-181X
Early Development, AstraZeneca R&D, Södertälje, Sweden.
Early Development, AstraZeneca R&D, Södertälje, Sweden.
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2007 (English)In: Journal of Organic Chemistry, ISSN 0022-3263, E-ISSN 1520-6904, Vol. 72, no 15, 5886-5889 p.Article in journal (Refereed) Published
Abstract [en]

(Chemical Equation Presented) Cyclization reactions involving cyanoacetylated bisindoles have been studied, providing access to various novel cyclohepta[2,1-b:3,4-b′]diindole derivatives as well as some related fused pentacyclic systems. Treatment of 3-cyanoacetyl-2,3′-diindolylmethane with methanesulfonic acid gave 6-(cyanomethyl)indolo[3,2-b]carbazole in a good yield.

Place, publisher, year, edition, pages
2007. Vol. 72, no 15, 5886-5889 p.
Keyword [en]
fused indole prepn, cycloheptadiindole prepn, oxido azepinodiindolone prepn, indolocarbazole prepn, cyanoacetyl biindole prepn cyclocondensation reaction
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-91997DOI: 10.1021/jo0706729ISI: 000247992800062OAI: oai:DiVA.org:kth-91997DiVA: diva2:511796
Note
CAPLUS AN 2007:678850(Journal). QC 20120327Available from: 2012-03-23 Created: 2012-03-23 Last updated: 2017-12-07Bibliographically approved

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Slätt, Johnny

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