Photoinduced Intramolecular Macrocyclization Reaction between a Bpa and a Met Residue in a Helical Peptide: 3D-Structures of the Diastereomeric Products. (Articolo in rivista)

Type
Label
  • Photoinduced Intramolecular Macrocyclization Reaction between a Bpa and a Met Residue in a Helical Peptide: 3D-Structures of the Diastereomeric Products. (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/chem.200802066 (literal)
Alternative label
  • Alessandro Moretto; Marco Crisma; Fernando Formaggio; Lawrence A. Huck; Dino Mangion; William J. Leigh; Claudio Toniolo (2009)
    Photoinduced Intramolecular Macrocyclization Reaction between a Bpa and a Met Residue in a Helical Peptide: 3D-Structures of the Diastereomeric Products.
    in Chemistry - A European Journal
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Alessandro Moretto; Marco Crisma; Fernando Formaggio; Lawrence A. Huck; Dino Mangion; William J. Leigh; Claudio Toniolo (literal)
Pagina inizio
  • 67 (literal)
Pagina fine
  • 70 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 15 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 1 (literal)
Note
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Chimica Biomolecolare, CNR, Unità di Padova, Dipartimento di Scienze Chimiche, Università di Padova, via Marzolo 1, 35131 Padova (Italy); Department of Chemistry, McMaster University, Hamilton, ON, L8S 4M1 (Canada) (literal)
Titolo
  • Photoinduced Intramolecular Macrocyclization Reaction between a Bpa and a Met Residue in a Helical Peptide: 3D-Structures of the Diastereomeric Products. (literal)
Abstract
  • The first photoinduced intramolecular macrocyclization reaction in a helical peptide, containing a Bpa and a Met residue incorporated one on top of the other after a complete turn of the helix, has been performed. The photochemical remote functionalization and subsequent intramolecular cross-linking are strictly regioselective, involving exclusively the original Met side-chain epislon-CH3 group and generating two diastereomeric macrocyclized peptides. (literal)
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