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Acid-induced dimerization of 3-(1H-indol-3-yl)maleimides. Formation of cyclopentindole derivatives
Södertörns högskola, Avdelning Naturvetenskap.
2000 (engelsk)Inngår i: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, ISSN 1470-4358, nr 16, s. 2615-2621Artikkel i tidsskrift (Fagfellevurdert) 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.

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2000. nr 16, s. 2615-2621
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URN: urn:nbn:se:sh:diva-15766DOI: 10.1039/b004030oISI: 000088767000010OAI: oai:DiVA.org:sh-15766DiVA, id: diva2:508031
Tilgjengelig fra: 2012-03-07 Laget: 2012-03-07 Sist oppdatert: 2012-03-07bibliografisk kontrollert

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