sh.sePublications
EnglishSvenskaNorsk
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
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, Vol. 57, no 7, 1273-1278 p.Article 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, 1273-1278 p.
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:sh:diva-15797DOI: 10.3987/COM-02-9477ISI: 000177219000010Scopus ID: 2-s2.0-0036646287OAI: oai:DiVA.org:sh-15797DiVA: diva2:508393
Available from: 2012-03-08 Created: 2012-03-07 Last updated: 2014-04-23Bibliographically approved

Open Access in DiVA

No full text

Other links

Publisher's full textScopus

Search in DiVA

By author/editor
Bergman, Jan
By organisation
Avdelning Naturvetenskap
In the same journal
Heterocycles
Organic Chemistry

Search outside of DiVA

GoogleGoogle Scholar

Altmetric score

Total: 62 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
v. 2.27.0
|
Södertörn University
|
Södertörn University Library
|
DiVA Login