New synthetic strategy for o-NBS protected amino acids and their use in synthesis of mono-benzylated peptides (447 views)
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: Not available.
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:
Sandler, R., (1983) Organic Functional Group Preparations, , 2nd ed. Academic Press New Yor
Marson, C.M., Hobson, A.D., (1995) Comprehensive Organic Functional Group Transformation, 2, p. 297. , A. Katritzky O. Meth-Cohn C.W. Rees Pergamon Press Oxford
Fukuyama, T., Jow, C.K., Cheung, M., (1995) Tetrahedron Lett., 36, pp. 6373-6374
Fukuyama, T., Cheung, M., Jow, C.K., Hidai, Y., Kan, T., (1997) Tetrahedron Lett., 38, pp. 5831-5834
Kurosawa, W., Kan, T., Fukuyama, T., (2002) Org. Synth., 79, pp. 186-195
Reichwein, J.F., Liskamp, R.M.J., (1998) Tetrahedron Lett., 39, pp. 1243-1246
Bodanszky, M., Bodanszky, A., (1994) The Practice of Peptide Synthesis, , 2nd ed. Springer New York, USA
Di Gioia, M.L., Leggio, A., Liguori, A., (2005) J. Org. Chem., 70, pp. 3892-3897
notenotenoteSheppard, R.C., Williams, B.J., (1982) Int. J. Peptide Protein Res., 20, pp. 451-454
Kaiser, E., Colescott, R.L., Bossinger, C.D., Cook, P.I., (1970) Anal. Biochem., 34, pp. 595-598
notenotenoteUR - http://www.scopus.com/inward/record.url?eid=2-s2.0-23944434415&partnerID=40&md5=b23b086fd196ad5bccf397542cce2672
Marson, C. M., Hobson, A. D., (1995) Comprehensive Organic Functional Group Transformation, 2, p. 297. , A. Katritzky O. Meth-Cohn C. W. Rees Pergamon Press Oxford
Reichwein, J. F., Liskamp, R. M. J., (1998) Tetrahedron Lett., 39, pp. 1243-1246
Di Gioia, M. L., Leggio, A., Liguori, A., (2005) J. Org. Chem., 70, pp. 3892-3897
Tetrahedron Lett (ISSN: 0040-4039), 2005 Sep 26; 46(39): 6637-6640.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 2.477, 5-year impact factor: 2.295
Url: Not available.
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:
Sandler, R., (1983) Organic Functional Group Preparations, , 2nd ed. Academic Press New Yor
Marson, C.M., Hobson, A.D., (1995) Comprehensive Organic Functional Group Transformation, 2, p. 297. , A. Katritzky O. Meth-Cohn C.W. Rees Pergamon Press Oxford
Fukuyama, T., Jow, C.K., Cheung, M., (1995) Tetrahedron Lett., 36, pp. 6373-6374
Fukuyama, T., Cheung, M., Jow, C.K., Hidai, Y., Kan, T., (1997) Tetrahedron Lett., 38, pp. 5831-5834
Kurosawa, W., Kan, T., Fukuyama, T., (2002) Org. Synth., 79, pp. 186-195
Reichwein, J.F., Liskamp, R.M.J., (1998) Tetrahedron Lett., 39, pp. 1243-1246
Bodanszky, M., Bodanszky, A., (1994) The Practice of Peptide Synthesis, , 2nd ed. Springer New York, USA
Di Gioia, M.L., Leggio, A., Liguori, A., (2005) J. Org. Chem., 70, pp. 3892-3897
notenotenoteSheppard, R.C., Williams, B.J., (1982) Int. J. Peptide Protein Res., 20, pp. 451-454
Kaiser, E., Colescott, R.L., Bossinger, C.D., Cook, P.I., (1970) Anal. Biochem., 34, pp. 595-598
notenotenoteUR - http://www.scopus.com/inward/record.url?eid=2-s2.0-23944434415&partnerID=40&md5=b23b086fd196ad5bccf397542cce2672
Marson, C. M., Hobson, A. D., (1995) Comprehensive Organic Functional Group Transformation, 2, p. 297. , A. Katritzky O. Meth-Cohn C. W. Rees Pergamon Press Oxford
Reichwein, J. F., Liskamp, R. M. J., (1998) Tetrahedron Lett., 39, pp. 1243-1246
Di Gioia, M. L., Leggio, A., Liguori, A., (2005) J. Org. Chem., 70, pp. 3892-3897
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.
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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14 Records (14 excluding Abstracts).
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Total 5 year impact factor: 50.849 (50.849 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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