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

Authors :
Eliana Di Carlo
Laura Belvisi
Carlo Scolastico
Matteo Colombo
Leonardo Manzoni
Alessandra Forni
Source :
Tetrahedron letters 45 (2004): 6311–6315. doi:10.1016/j.tetlet.2004.06.077, info:cnr-pdr/source/autori:Manzoni L.; Belvisi L.; Colombo M.; Di Carlo E.; Forni A.; Scolastico C./titolo:Stereoselective synthesis of C-alpha-tetrasubstituted azabicyclo[X.3.0]alkane amino acids/doi:10.1016%2Fj.tetlet.2004.06.077/rivista:Tetrahedron letters/anno:2004/pagina_da:6311/pagina_a:6315/intervallo_pagine:6311–6315/volume:45
Publication Year :
2004
Publisher :
Pergamon Press, Frankfurt , Regno Unito, 2004.

Abstract

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

Details

Language :
English
Database :
OpenAIRE
Journal :
Tetrahedron letters 45 (2004): 6311–6315. doi:10.1016/j.tetlet.2004.06.077, info:cnr-pdr/source/autori:Manzoni L.; Belvisi L.; Colombo M.; Di Carlo E.; Forni A.; Scolastico C./titolo:Stereoselective synthesis of C-alpha-tetrasubstituted azabicyclo[X.3.0]alkane amino acids/doi:10.1016%2Fj.tetlet.2004.06.077/rivista:Tetrahedron letters/anno:2004/pagina_da:6311/pagina_a:6315/intervallo_pagine:6311–6315/volume:45
Accession number :
edsair.doi.dedup.....5525fd754c91695b00edfa6a6feb3c7f