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 The Role of the Amino Protecting Group during Parahydrogenation of Protected Dehydroamino Acids (85 visite)
Cerutti E, Viale A, Nervi C, Gobetto R, Aime S
J Phys Chem A (ISSN: 1520-5215electronic, 1089-5639linking), 2015 Nov 19; 119(46): 11271-11279.Tipo di articolo: Abstract, Journal Article, Impact factor: 2.883, Impact factor a 5 anni: 2.709Url: Non disponibile.Parole chiave: Non disponibili.Affiliazioni:
*** IBB - CNR ***
Department of Molecular Biotechnologies and Health Sciences, University of Torino , Via Nizza 52, 10126 Torino, Italy., Riferimenti:
Non disponibile. A series of dehydroamino acids endowed with different protective groups at the amino and carboxylate moieties and with different substituents at the double bond have been reacted with parahydrogen. The observed ParaHydrogen Induced Polarization (PHIP) effects in the (1)H NMR spectra are strongly dependent on the amino protecting group. DFT calculations allowed us to establish a relationship between the structures of the reaction intermediates (whose energies depend on the amido substitution) and the observed PHIP patterns.
Roviello GN, Crescenzo C, Capasso D, Di Gaetano S, Franco S, Bucci EM, Pedone C* Synthesis of a novel Fmoc-protected nucleoaminoacid for the solid phase assembly of 4-piperidyl glycine/L-arginine-containing nucleopeptides and preliminary RNA interaction studies (134 visite)Amino Acids (ISSN: 0939-4451, 1438-2199, 1438-2199electronic), 2010 Sep; 39(3): 795-800.Impact Factor: 4.106Dettagli Esporta in BibTeX Esporta in EndNoteRoviello GN, Gröschel S, Pedone C, Diederichsen U * Synthesis of novel MMT/acyl-protected nucleo alanine monomers for the preparation of DNA/alanyl-PNA chimeras (108 visite)Amino Acids (ISSN: 1438-2199, 0939-4451, 1438-2199electronic), 2010 May; 38(5): 1301-1309.Impact Factor: 4.106Dettagli Esporta in BibTeX Esporta in EndNoteRoviello GN, Gröschel S, Pedone C, Diederichsen U * Erratum: Synthesis of novel MMT/acyl-protected nucleo alanine monomers for the preparation of DNA/alanyl-PNA chimeras (Amino Acids DOI: 10. 1007/s00726-009-0324-x) (110 visite)Amino Acids (ISSN: 0939-4451, 1438-2199, 1438-2199electronic), 2010; 38(5): 1311-1312.Impact Factor: 4.106Dettagli Esporta in BibTeX Esporta in EndNoteJoszal V, Nagy Z, Osz K, Sanna D, Di Natale G, La Mendola D, Pappalardo G, Rizzarelli E, Sovago I * Transition metal complexes of terminally protected peptides containing histidyl residues (155 visite)J Chem Res (ISSN: 0162-0134, 1873-3344, 0162-0134print), 2006 Sep; 100(8): 1399-1409.Impact Factor: 2.654Dettagli Esporta in BibTeX Esporta in EndNoteDe Luca S, Della Moglie R, De Capua A, Morelli G* New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides (144 visite)Tetrahedron Lett (ISSN: 0040-4039), 2005 Sep 26; 46(39): 6637-6640.Impact Factor: 2.477Dettagli Esporta in BibTeX Esporta in EndNoteBenedetti E, Iacovino R, Pedone C, Rossi F, Saviano M, Isernia C, Montesarchio D, DeNapoli L, Piccialli G β-Amino acid residues: Conformational characterization of an N- and C-protected homo-β-(S)-leucine (87 visite)Int J Pept Res Ther (ISSN: 0929-5666, 1573-3149), 1997 Jun; 4(3): 129-134.Impact Factor: 0.557Dettagli Esporta in BibTeX Esporta in EndNote6 Records ( 6 escludendo Abstract e Conferenze). Impact factor totale: 18.006 ( 18.006 escludendo Abstract e Conferenze). Impact factor a 5 anni totale: 17.341 ( 17.341 escludendo Abstract e Conferenze). Ultima modifica di Gennaro Angrisano in data Wednesday 09 December 2015, 11:06:20 85 visite. Ultima visita in data Saturday 29 December 2018, 9:23:15
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