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Acid-induced dimerization of 3-(1H-indol-3-yl)maleimides. Formation of cyclopentindole derivatives
Södertörn University, Avdelning Naturvetenskap.
2000 (English)In: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, ISSN 1470-4358, no 16, 2615-2621 p.Article in journal (Refereed) Published
Abstract [en]

Acid-induced dimerizations of 3-substituted maleimides have been investigated, leading to e.g. the cyclopentindole 9 and the deeply coloured spiro compounds 24 and 25 in good yields. 3-(1H-Indol-3-yl)maleimide 6b readily gave the cycloaddition products 13-15 on treatment with appropriate dienophiles. In addition, several related 3,3-di-(1H-indol-3-yl)succinimides have been prepared and studied.

Place, publisher, year, edition, pages
2000. no 16, 2615-2621 p.
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:sh:diva-15766DOI: 10.1039/b004030oISI: 000088767000010OAI: oai:DiVA.org:sh-15766DiVA: diva2:508031
Available from: 2012-03-07 Created: 2012-03-07 Last updated: 2012-03-07Bibliographically approved

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Bergman, Jan
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Avdelning Naturvetenskap
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