New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides
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New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides
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688 views
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De Luca S
, Della Moglie R, De Capua A,
Morelli G
Tetrahedron Lett (ISSN: 0040-4039)
,
2005 Sep 26;
46(39): 6637-6640.
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Paper type:
Journal Article
Impact factor:
2.477,
5-year impact factor:
2.295
Url:
https://www.scopus.com/inward/record.uri?eid=2-s2.0-23944434415&doi=10.1016%2fj.tetlet.2005.07.154&partnerID=40&md5=905f7883ebb08f5263e0c5507888e400
Keywords:
Building Blocks For Peptide Synthesis, Mono-Benzylated Peptides, O-Nbs Protected Amino Acids, 2 Nitrobenzenesulfonamide, Amino Acid Derivative, Benzenesulfonamide Derivative, Unclassified Drug, Article, Benzylation, Solid Phase Synthesis
Affiliations:
*** IBB - CNR ***
Department of Biological Sciences, Biostructures Section, University of Naples 'Federico II', via Mezzocannone, 16, Naples I-80134, Italy
References:
Not available.
New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides
A synthetic strategy to prepare o-NBS protected Fmoc-amino acids under mild conditions, in a rapid and efficient way, characterised by high yields and excellent purity of the final products has been developed. The o-NBS protected Fmoc-amino acids are employed in solid phase peptide synthesis to prepare peptidomimetics carrying mono-benzylated moieties on peptide side chains. © 2005 Elsevier Ltd. All rights reserved.
New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides
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New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides
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Angeli A,
Buonanno M
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Leiria Campo V, Riul TB, Oliveira Bortot L, Martins-teixeira MB, Fiori Marchiori M,
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Palmieri M, Russo L, Malgieri G, Esposito S, Baglivo I, Rivellino A, Farina B, de Paola I,
Zaccaro L
, Milardi D, Isernia C, Pedone PV, Fattorusso R
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Roviello GN
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Accardo A
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Squeglia F
, Marchetti R,
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Roviello GN
, Crescenzo C, Capasso D,
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, Franco S, Bucci EM,
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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
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Roviello GN
, Moccia M, Sapio R, Valente M, Bucci EM, Castiglione M,
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Vander Borght T, Asenbaum S, Bartenstein P, Halldin C, Kapucu O, Van Laere K, Varrone A, Tatsch K
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EANM procedure guidelines for brain tumour imaging using labelled amino acid analogues
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D'Amore M,
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*
Conformational behavior and magnetic properties of a nitroxide amino acid derivative in vacuo and in aqueous solution
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Peggion C, Formaggio F, Crisma M, Toniolo C, Jimenez AI, Cativiela C, Kaptein B, Broxterman QB, Saviano M, Benedetti E
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Folding of peptides characterized by c3Val, a highly constrained analogue of valine
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Crisma M, Formaggio F, Valle G, Toniolo C, Saviano M, Iacovino R,
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14
Records (
14
excluding Abstracts).
Total impact factor:
51.35
(
51.35
excluding Abstracts).
Total 5 year impact factor:
50.849
(
50.849
excluding Abstracts).
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Marco Comerci
on Tuesday 09 April 2024, 12:56:56
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