http://www.cnr.it/ontology/cnr/individuo/prodotto/ID14740
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
- Pagina fine
- 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
- 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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