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
Synthesis of N-H vinylaziridines: a comparative study
Royal Institute of Technology, Sweden.
Royal Institute of Technology, Sweden.
Royal Institute of Technology, Sweden.
2002 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 58, no 30, 5979-5982 p.Article in journal (Refereed) Published
Abstract [en]

Vinylaziridines are useful and versatile synthetic intermediates, as the relief of ring-strain provides a driving force for efficient ring-opening or ring-expansion reactions. Furthermore, the vinyl group can be derivatized into interesting functionalities. The ring-closure of vicinal amino alcs. constitutes a straightforward route to aziridines. Several methods exist for this transformation, although many cannot be applied to vinylaziridines due to their acid lability. This comparative study describes the most effective sequences for the formation of N-H vinylaziridines.

Place, publisher, year, edition, pages
2002. Vol. 58, no 30, 5979-5982 p.
Keyword [en]
amino alcohols, vinylaziridines, ring-closure
National Category
Organic Chemistry
Research subject
Organic Chemistry
Identifiers
URN: urn:nbn:se:su:diva-109688DOI: 10.1016/S0040-4020(02)00610-5ISI: 000177028600002OAI: oai:DiVA.org:su-109688DiVA: diva2:766457
Available from: 2014-11-27 Created: 2014-11-27 Last updated: 2017-12-05Bibliographically approved

Open Access in DiVA

fulltext(339 kB)92 downloads
File information
File name FULLTEXT01.pdfFile size 339 kBChecksum SHA-512
8c4a83f3bc6c22fda1382428a8805d68161c95c865bf41b779de36aa4707422dabe120adf1eefeed0e442c2db5d5db1c09b433f0d1e4b2ce30ccdb975c786686
Type fulltextMimetype application/pdf

Other links

Publisher's full text

Search in DiVA

By author/editor
Olofsson, Berit
In the same journal
Tetrahedron
Organic Chemistry

Search outside of DiVA

GoogleGoogle Scholar
Total: 92 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 76 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