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Oxygenation of 2,3-dihydroindoles.
Unit for Organic Chemistry, Department of Biosciences, Karolinska Institute and Södertörn University College, Novum Research Park.ORCID iD: 0000-0002-8444-181X
Unit for Organic Chemistry, Department of Biosciences, Karolinska Institute and Södertörn University College, Novum Research Park.
2002 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 58, no 45, 9187-9191 p.Article in journal (Refereed) Published
Abstract [en]

Indolines (2,3-dihydroindoles) and isatogens (3-oxo-3H-indole 1-oxides) have been prepd. in an efficient route starting from indoles substituted in position 2. Redn. of the 2-substituted indoles was performed with tin and hydrochloric acid to give racemic indolines, which were converted to isatogens by 3-chloroperoxybenzoic acid (m-CPBA). [on SciFinder(R)]

Place, publisher, year, edition, pages
2002. Vol. 58, no 45, 9187-9191 p.
Keyword [en]
redn indole, indoline prepn oxidn, isatogen prepn
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-92003DOI: 10.1016/S0040-4020(02)01198-5OAI: oai:DiVA.org:kth-92003DiVA: diva2:511784
Note
CAPLUS AN 2002:831397(Journal) NR 20140805Available from: 2012-03-23 Created: 2012-03-23 Last updated: 2017-12-07Bibliographically approved

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