An easy and general azidolysis of vinylepoxides mediated by BF3 center dot OEt2 and TMSN3 recently reported by our group has been extended to vinylaziridines. The reaction affords unsaturated azido derivatives with complete stereoselectivity and regioselectivity, when in the presence of electron-poor olefins, regardless of the size of substituents on the heterocyclic ring.

BF3 center dot OEt2/TMSN3 Mediated Regioselective Azidolysis of Vinylaziridines

Righi Giuliana;Bovicelli Paolo;
2012

Abstract

An easy and general azidolysis of vinylepoxides mediated by BF3 center dot OEt2 and TMSN3 recently reported by our group has been extended to vinylaziridines. The reaction affords unsaturated azido derivatives with complete stereoselectivity and regioselectivity, when in the presence of electron-poor olefins, regardless of the size of substituents on the heterocyclic ring.
2012
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
vinylepoxides
vinylaziridines
azidolysis
azido alcohols
azido amines
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/223235
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact