메뉴 건너뛰기




Volumn 3, Issue 6, 1997, Pages 429-441

Triphosgene: An efficient carbonylating agent for liquid and solid-phase aza-peptide synthesis. Application to the synthesis of two aza-analogues of the AChR MIR decapeptide

Author keywords

Aza alanine; Aza asparagine; Aza aspartic acid; Aza peptides; Triphosgene

Indexed keywords

BIS(TRICHLOROMETHYL) CARBONATE; CHOLINERGIC RECEPTOR; DRUG DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; EPITOPE; HETEROCYCLIC COMPOUND; OLIGOPEPTIDE; PHOSGENE;

EID: 0031263756     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1387(199711)3:6<429::AID-PSC115>3.0.CO;2-C     Document Type: Article
Times cited : (28)

References (21)
  • 2
    • 0012771519 scopus 로고
    • Synthese von eledoisin-octapeptiden mit den carbazylresten azaglycin und α-azaasparagin statt glycin und asparagin
    • H. Niedrich and C. Oehme (1972). Synthese von eledoisin-octapeptiden mit den carbazylresten azaglycin und α-azaasparagin statt glycin und asparagin. J. Prakt. Chem. 314, 759-768.
    • (1972) J. Prakt. Chem. , vol.314 , pp. 759-768
    • Niedrich, H.1    Oehme, C.2
  • 3
    • 84981758430 scopus 로고
    • Uber neuartige azapeptide
    • J. Gante (1965). Uber neuartige azapeptide. Chem. Ber. 98, 540-547.
    • (1965) Chem. Ber. , vol.98 , pp. 540-547
    • Gante, J.1
  • 4
    • 85082699866 scopus 로고
    • Azapeptides
    • J. Gante (1989). Azapeptides. Synthesis, 405-413.
    • (1989) Synthesis , pp. 405-413
    • Gante, J.1
  • 5
    • 0016417266 scopus 로고
    • Polypeptides. Part XIII. Preparation of α-aza-amino-acid (carbazic acid) derivatives and intermediates for the preparation of α-aza-peptides
    • A. S. Dutta and J. S. Morley (1975). Polypeptides. Part XIII. Preparation of α-aza-amino-acid (carbazic acid) derivatives and intermediates for the preparation of α-aza-peptides. J. Chem. Soc. Perkin Trans. I, 1712-1720.
    • (1975) J. Chem. Soc. Perkin Trans. I , pp. 1712-1720
    • Dutta, A.S.1    Morley, J.S.2
  • 6
    • 0028038601 scopus 로고
    • Peptidomimetics-tailored enzyme inhibitors
    • J. Gante (1994). Peptidomimetics-tailored enzyme inhibitors. Angew. Chem. Int. Ed. Engl. 33, 1699-1720.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1699-1720
    • Gante, J.1
  • 8
    • 0026806775 scopus 로고
    • The couple Pro/AzaPro: A means of β-turn formation control. Synthesis and conformation of two AzaPro-containing dipeptides
    • A. Lecoq, G. Boussard, M. Marraud and A. Aubry (1992). The couple Pro/AzaPro: A means of β-turn formation control. Synthesis and conformation of two AzaPro-containing dipeptides. Tetrahedron Lett. 33, 5209-5212.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 5209-5212
    • Lecoq, A.1    Boussard, G.2    Marraud, M.3    Aubry, A.4
  • 9
    • 0026496927 scopus 로고
    • Incorporation of azaglutamine residues into peptides synthesized by the ultra-high load solid (gel)-phase technique
    • C. J. Gray, M. Quibell, N. Baggett and T. Hammerle (1992). Incorporation of azaglutamine residues into peptides synthesized by the ultra-high load solid (gel)-phase technique. Int. J. Peptide Protein Res. 40, 351-362.
    • (1992) Int. J. Peptide Protein Res. , vol.40 , pp. 351-362
    • Gray, C.J.1    Quibell, M.2    Baggett, N.3    Hammerle, T.4
  • 10
    • 37049076684 scopus 로고
    • Synthesis of azapeptides by the Fmoc/tert-butyl/-polyamide technique
    • M. Quibell, W. G. Turnell and T. Johnson (1993). Synthesis of azapeptides by the Fmoc/tert-butyl/-polyamide technique. J. Chem. ,Soc. Perkin Trans. I, 2843-2849.
    • (1993) J. Chem. ,Soc. Perkin Trans. I , pp. 2843-2849
    • Quibell, M.1    Turnell, W.G.2    Johnson, T.3
  • 11
    • 0025969056 scopus 로고
    • Synthesis and spectroscopic properties of azaglutamine amino acid and peptide derivatives
    • C. J. Gray, M. Quibell, K.-L. Jiang and N. Baggett (1991). Synthesis and spectroscopic properties of azaglutamine amino acid and peptide derivatives. Synthesis 3, 141-146.
    • (1991) Synthesis , vol.3 , pp. 141-146
    • Gray, C.J.1    Quibell, M.2    Jiang, K.-L.3    Baggett, N.4
  • 12
    • 0000572473 scopus 로고
    • Preparation and properties of some aza-amino-acid derivatives; their possible use in peptide synthesis
    • C. J. Gray, J. C. Ireson and R. C. Parker (1977). Preparation and properties of some aza-amino-acid derivatives; their possible use in peptide synthesis. Tetrahedron 33, 739-743.
    • (1977) Tetrahedron , vol.33 , pp. 739-743
    • Gray, C.J.1    Ireson, J.C.2    Parker, R.C.3
  • 13
    • 0029295118 scopus 로고
    • Synthesis and properties of the first all-aza analogue of a biologically active peptide
    • J. Gante, M. Krug, G. Lauterbach, R. Weitzel and W. Hiller (1995). Synthesis and properties of the first all-aza analogue of a biologically active peptide. J. Peptide Sci. 2, 201-206.
    • (1995) J. Peptide Sci. , vol.2 , pp. 201-206
    • Gante, J.1    Krug, M.2    Lauterbach, G.3    Weitzel, R.4    Hiller, W.5
  • 14
    • 0000893702 scopus 로고
    • Synthesis and properties of 1-acetyl-2-benzyl carbazate, an analog of acetyl-D- and L-phenylalanine ethyl ester
    • A. N. Kurtz and C. Niemann (1961). Synthesis and properties of 1-acetyl-2-benzyl carbazate, an analog of acetyl-D- and L-phenylalanine ethyl ester. J. Org. Chem. 26, 1843-1846.
    • (1961) J. Org. Chem. , vol.26 , pp. 1843-1846
    • Kurtz, A.N.1    Niemann, C.2
  • 17
    • 84985534727 scopus 로고
    • Triphosgene, a crystalline phosgene substitute
    • H. Eckert and B. Forster (1987). Triphosgene, a crystalline phosgene substitute. Angew. Chem. Int. Ed. Engl. 26, 894-895.
    • (1987) Angew. Chem. Int. Ed. Engl. , vol.26 , pp. 894-895
    • Eckert, H.1    Forster, B.2
  • 20
    • 0030068665 scopus 로고    scopus 로고
    • Crystal structures of peptides and modified peptides
    • M. Marraud and A. Aubry (1996). Crystal structures of peptides and modified peptides. Biopolym (Peptide Sci.) 40, 45-83.
    • (1996) Biopolym (Peptide Sci.) , vol.40 , pp. 45-83
    • Marraud, M.1    Aubry, A.2
  • 21
    • 0001707341 scopus 로고
    • Localization of the main immunogenic region of human muscle acetylcholine receptor to residues 67-76 of the α-subunit
    • S. J. Tzartos, A. Kokla, S. Walgrave and B. Contitronconi (1988). Localization of the main immunogenic region of human muscle acetylcholine receptor to residues 67-76 of the α-subunit. Proc. Natl. Acad. Sci. USA 85, 2899-2903.
    • (1988) Proc. Natl. Acad. Sci. USA , vol.85 , pp. 2899-2903
    • Tzartos, S.J.1    Kokla, A.2    Walgrave, S.3    Contitronconi, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.