Oxygenation of 2,3-dihydroindoles.
2002 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 58, no 45, 9187-9191 p.Article in journal (Refereed) Published
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.
redn indole, indoline prepn oxidn, isatogen prepn
IdentifiersURN: urn:nbn:se:kth:diva-92003DOI: 10.1016/S0040-4020(02)01198-5OAI: oai:DiVA.org:kth-92003DiVA: diva2:511784
CAPLUS AN 2002:831397(Journal) NR 201408052012-03-232012-03-232012-03-23Bibliographically approved