Glycal-mediated synthesis of enantiomerically pure 5-substituted isoxazoles containing a differentially O-benzylated glycerol moiety (Articolo in rivista)

Type

• Prodotto della ricerca (Classe)
• Articolo in rivista (Classe)

Label

• Glycal-mediated synthesis of enantiomerically pure 5-substituted isoxazoles containing a differentially O-benzylated glycerol moiety (Articolo in rivista) (literal)

Anno

• 2002-01-01T00:00:00+01:00 (literal)

Alternative label

• Piancatelli G., Weinig H.G., Colapietro G., Passacantilli P. (2002)
  Glycal-mediated synthesis of enantiomerically pure 5-substituted isoxazoles containing a differentially O-benzylated glycerol moiety
  in Tetrahedron letters
  (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

• Piancatelli G., Weinig H.G., Colapietro G., Passacantilli P. (literal)

Pagina inizio

• 4613 (literal)

Pagina fine

• 4615 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume

• 43 (literal)

Rivista

• Tetrahedron letters (Rivista)

Note

• ISI Web of Science (WOS) (literal)

Titolo

• Glycal-mediated synthesis of enantiomerically pure 5-substituted isoxazoles containing a differentially O-benzylated glycerol moiety (literal)

Abstract

• A short, glycal-mediated synthesis of new chiral 5-substituted isoxazole bearing a differentially O-protected glycerol moiety in the side chain has been accomplished. An X-ray crystallographic structural analysis confirmed the structural assignment of the new product (literal)

Prodotto di

• Institute of biomolecular chemistry (ICB) (Istituto)

Incoming links:

Prodotto

• Institute of biomolecular chemistry (ICB) (Istituto)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• Tetrahedron letters (Rivista)