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Oxidative coupling of indoline-2-thione or oxindole: Formation of cyclic and acyclic indole trimers
Södertörn University, Avdelning Naturvetenskap. Karolinska Institute.
2002 (English)In: Heterocycles, ISSN 0385-5414, E-ISSN 1881-0942, Vol. 57, no 7, p. 1273-1278Article in journal (Refereed) Published
Abstract [en]

Oxidation of indoline-2-thione using p-toluenesulfonyl azide produced a modest yield of the structurally novel cyclic sulfur containing indole trimer (12). In contrast, the oxidation of oxindole with iodine instead produced an acyclic trimeric indole derivative.
Place, publisher, year, edition, pages
2002. Vol. 57, no 7, p. 1273-1278
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Organic Chemistry
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URN: urn:nbn:se:sh:diva-15797DOI: 10.3987/COM-02-9477ISI: 000177219000010Scopus ID: 2-s2.0-0036646287OAI: oai:DiVA.org:sh-15797DiVA, id: diva2:508393
Available from: 2012-03-08 Created: 2012-03-07 Last updated: 2017-12-07Bibliographically approved

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Bergman, Jan

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