4-Amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic acid (beta-TOAC), the first spin-labelled, cyclic, chiral beta-amino acid resolved in an enantiomerically pure state (Articolo in rivista)

Type
Label
  • 4-Amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic acid (beta-TOAC), the first spin-labelled, cyclic, chiral beta-amino acid resolved in an enantiomerically pure state (Articolo in rivista) (literal)
Anno
  • 2003-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/S0040-4039(03)00572-0 (literal)
Alternative label
  • Wright K., Crisma M., Toniolo C., Török R., Péter A., Wakselman M., Mazaleyrat J.P. (2003)
    4-Amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic acid (beta-TOAC), the first spin-labelled, cyclic, chiral beta-amino acid resolved in an enantiomerically pure state
    in Tetrahedron letters
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Wright K., Crisma M., Toniolo C., Török R., Péter A., Wakselman M., Mazaleyrat J.P. (literal)
Pagina inizio
  • 3381 (literal)
Pagina fine
  • 3384 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • Citazioni WOS: 21 Impact Factor 2003: 2.326 Coautore (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 44 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • SIRCOB, UMR CNRS 8086, Bat. Lavoisier, University of Versailles, 78000 Versailles, France; Institute of Biomolecular Chemistry, CNR, Department of Organic Chemistry, University of Padova, 35131 Padova, Italy; Department of Inorganic and Analytical Chemistry, University of Szeged, H-6701 Szeged, Hungary (literal)
Titolo
  • 4-Amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic acid (beta-TOAC), the first spin-labelled, cyclic, chiral beta-amino acid resolved in an enantiomerically pure state (literal)
Abstract
  • Amination of 3-carboxymethyl-1-oxyl-2,2,6,6-tetramethyl-4-piperidone with (R)-alpha-methylbenzylamine, NaBH3CN reduction of the resulting enamine and removal of the chiral auxiliary from the separated diastereoisomers, led to enantiomerically pure (3S,4S) and (3R,4R) methyl 4-amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylates. (literal)
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Autore CNR

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