By a stereoselective alkylation approach a synthesis of eight enantiopure, sterically constrained C-alpha-tetrasubstituted azabicycloalkane amino acids was carried out.

Stereoselective synthesis of C-alpha-tetrasubstituted azabicyclo[X.3.0]alkane amino acids / L. Manzoni, L. Belvisi, M. Colombo, E. Di Carlo, A. Forni, C. Scolastico. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 45:33(2004), pp. 6311-6315.

Stereoselective synthesis of C-alpha-tetrasubstituted azabicyclo[X.3.0]alkane amino acids

L. Belvisi
Secondo
;
M. Colombo;E. Di Carlo;C. Scolastico
Ultimo
2004

Abstract

By a stereoselective alkylation approach a synthesis of eight enantiopure, sterically constrained C-alpha-tetrasubstituted azabicycloalkane amino acids was carried out.
Alkylation; Bicyclic aliphatic compounds; Enolates; Lactams; Peptidomimetics
Settore CHIM/06 - Chimica Organica
2004
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

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/2434/144069
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 9
social impact