http://www.cnr.it/ontology/cnr/individuo/prodotto/ID287571
A Quaternary Nitronyl Nitroxide alpha-Amino Acid: Synthesis, Configurational and Conformational Assignments, and Physicochemical Properties (Articolo in rivista)
- Type
- Label
- A Quaternary Nitronyl Nitroxide alpha-Amino Acid: Synthesis, Configurational and Conformational Assignments, and Physicochemical Properties (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejoc.201301765 (literal)
- Alternative label
Wright, K.; d'Aboville, E.; Scola, J.; Margola, T.; Toffoletti, A.; De Zotti, M.; Crisma, M.; Formaggio, F.; Toniolo, C. (2014)
A Quaternary Nitronyl Nitroxide alpha-Amino Acid: Synthesis, Configurational and Conformational Assignments, and Physicochemical Properties
in European journal of organic chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Wright, K.; d'Aboville, E.; Scola, J.; Margola, T.; Toffoletti, A.; De Zotti, M.; Crisma, M.; Formaggio, F.; Toniolo, C. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- ILV, UMR 8180, University of Versailles, 78035 Versailles, France;
GEMAC, UMR 8635, University of Versailles, 78035 Versailles, France;
Department of Chemistry, University of Padova, 35131 Padova, Italy;
Institute of Biomolecular Chemistry, Padova Unit, CNR, 35131 Padova, Italy (literal)
- Titolo
- A Quaternary Nitronyl Nitroxide alpha-Amino Acid: Synthesis, Configurational and Conformational Assignments, and Physicochemical Properties (literal)
- Abstract
- To expand the presently extremely limited repertoire of known nitronyl nitroxide -amino acids, we report here the synthesis of a novel, conformationally constrained, quaternary, chiral residue, Aic(CN), and its subsequent conversion into a blue-colored, imidazolinyl nitronyl nitroxide-bearing -amino acid, Aic(NN). Deprotection and peptide coupling reactions were examined. The configurational assignment of Aic(NN) was achieved by X-ray crystallographic analysis of an appropriate tripeptide. This latter investigation, accompanied by an IR absorption conformational analysis, strongly supports the view that the Aic(NN) residue is an efficient peptide turn former. Numerous spectroscopic and magnetic properties of its derivatives and the tripeptide are also described. Of particular relevance for future applications are its UV/Vis absorption, NMR, and EPR signatures. (literal)
- Prodotto di
- Autore CNR
- Insieme di parole chiave
Incoming links:
- Autore CNR di
- Prodotto
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
- Insieme di parole chiave di