uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • 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
Pyrrolidines from olefins via radical cyclization
Uppsala University.
Uppsala University.
Uppsala University.
1998 (English)In: TETRAHEDRON LETTERS, Vol. 39, no 16, 2429-2432 p.Other (Other scientific)
Abstract [en]

2,4-Disubstituted N-tosylpyrrolidines were prepared from olefins via N-tosylaziridination, benseneselenolate ring-opening and reductive radical cyclization. Azidoselenation of olefins, followed by reduction, N-tosylation, N-allylation and reductive radic

Place, publisher, year, pages
PERGAMON-ELSEVIER SCIENCE LTD , 1998. Vol. 39, no 16, 2429-2432 p.
Keyword [en]
RATE CONSTANTS; RING-CLOSURE; HETEROCYCLES; CARBON; IMINES
Identifiers
URN: urn:nbn:se:uu:diva-84799OAI: oai:DiVA.org:uu-84799DiVA: diva2:112707
Note
Addresses: Engman L, Uppsala Univ, Inst Chem, Dept Organ Chem, Box 531, S-75121 Uppsala, Sweden. Uppsala Univ, Inst Chem, Dept Organ Chem, S-75121 Uppsala, Sweden.Available from: 2008-10-17 Created: 2008-10-17

Open Access in DiVA

No full text

By organisation
Uppsala University

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 508 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • 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