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On the preparation of 1,2,5-selenadiazolo [3,4-e]indole and its [3,4-f] and [3,4-g] isomers through the Batcho-Leimgruber indole synthesis
Södertörn University, Avdelning Naturvetenskap.
Södertörn University, Avdelning Naturvetenskap.
2001 (English)In: ARKIVOC, ISSN 1551-7004, E-ISSN 1551-7012, Vol. 2, no 1, 136-142 p.Article in journal (Refereed) Published
Abstract [en]

1,2,5-Selenadiazolo[3,4-e]indole 6 was prepared by applying the Batcho-Leimgruber indole synthesis on 4-methyl-5-nitro-2,1,3-benzoselenadiazole 9. This methodology was unsuccessful when applied to 5-methyl-6-nitro-2,1,3-benzoselenadiazole 14 for the synthesis of 1,2,5-selenadiazolo[3,4-f]indole 5. An improvement on the preparation of 1,2,5-selenadiazolo[3,4-g]indole 3 is reported. An initial study on the bromination of 3 and the Se-77-NMR chemical shifts of 3 and 6, and of their precursors are presented.

Place, publisher, year, edition, pages
2001. Vol. 2, no 1, 136-142 p.
National Category
Chemical Sciences
URN: urn:nbn:se:sh:diva-15879ISI: 000171138800007ScopusID: 2-s2.0-3042698265OAI: diva2:509034
Available from: 2012-03-12 Created: 2012-03-09 Last updated: 2014-04-23Bibliographically approved

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