A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids (Articolo in rivista)

Type
Label
  • A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tetasy.2007.10.027 (literal)
Alternative label
  • Reginato G.; Di Credico B.; Andreotti D.; Mingardi A.; Paio A.; Donati D. (2007)
    A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids
    in Tetrahedron: asymmetry (Online)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Reginato G.; Di Credico B.; Andreotti D.; Mingardi A.; Paio A.; Donati D. (literal)
Pagina inizio
  • 2680 (literal)
Pagina fine
  • 2688 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 18 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 9 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Andreotti D.; Mingardi A.; Paio A.; Donati D. GlaxoSmithKline, Medicine Research Centre, Via A. Fleming 4, 37135 Verona, Italy (literal)
Titolo
  • A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids (literal)
Abstract
  • A highly stereoselective approach to 1,3,4,5- and 1,3,30,4,5-polysubstituted 2-oxopiperazines is reported. The method is based on the synthetic elaboration of naturally occurring amino acids to obtain enantiomerically enriched C-5 substituted oxopiperazines, which are further functionalized at C-3 via enolate formation and reaction with electrophiles. Notably, the two nitrogens of the ring can be orthogonally protected. (literal)
Prodotto di
Autore CNR

Incoming links:


Prodotto
Autore CNR di
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
data.CNR.it