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Volumn 6, Issue 5, 2000, Pages 243-250

Solid phase synthesis of C-terminal peptide amides: Development of a new aminoethyl-polystyrene linker on the Multipin(TM) solid support

Author keywords

Acetophenone based linker; Aminoethyl polystyrene; Multipin solid support; Solid phase synthesis of peptide amide

Indexed keywords

AMIDE; DICHLOROMETHANE; PEPTIDE; POLYESTER; TRIFLUOROACETIC ACID;

EID: 0034021915     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1387(200005)6:5<243::AID-PSC251>3.0.CO;2-4     Document Type: Article
Times cited : (2)

References (15)
  • 1
    • 85006883875 scopus 로고    scopus 로고
    • Solution phase synthesis of immunoregulating peptides. PCT Int. Appl. WO 9626955, 1996
    • Vladislav DV, Marxovich KA. Solution phase synthesis of immunoregulating peptides. PCT Int. Appl. WO 9626955, 1996.
    • Vladislav, D.V.1    Marxovich, K.A.2
  • 2
    • 0023391680 scopus 로고
    • An acid-labile anchoring linkage for solid-phase synthesis of C-terminal peptide amides under mild conditions
    • and references therein
    • Fernando A, Barany G. An acid-labile anchoring linkage for solid-phase synthesis of C-terminal peptide amides under mild conditions. Int. J. Peptide Protein Res. 1987; 30: 206-216 and references therein.
    • (1987) Int. J. Peptide Protein Res. , vol.30 , pp. 206-216
    • Fernando, A.1    Barany, G.2
  • 3
    • 0342862948 scopus 로고
    • Study of benzhydrylamine-type polymers. Synthesis and use of p-methoxybenzhydrylamine resin in the solid-phase preparation of peptides
    • Orlowski RC, Walter R, Winkler D. Study of benzhydrylamine-type polymers. Synthesis and use of p-methoxybenzhydrylamine resin in the solid-phase preparation of peptides. J. Org. Chem. 1976; 41: 3701-3705.
    • (1976) J. Org. Chem. , vol.41 , pp. 3701-3705
    • Orlowski, R.C.1    Walter, R.2    Winkler, D.3
  • 4
    • 1642593944 scopus 로고
    • Amide protection and amide supports in solid-phase peptide synthesis
    • Pietta PG, Marshall GR. Amide protection and amide supports in solid-phase peptide synthesis. J. Chem. Soc. D 1970; 11: 650-651.
    • (1970) J. Chem. Soc. D , vol.11 , pp. 650-651
    • Pietta, P.G.1    Marshall, G.R.2
  • 5
    • 45949123116 scopus 로고
    • Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methyl ester resin
    • Rink H. Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methyl ester resin. Tetrahedron Lett. 1987; 28: 3787-3790.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 3787-3790
    • Rink, H.1
  • 6
    • 0026532674 scopus 로고
    • Preparation of protected peptide amides using the Fmoc chemical protocol. Comparision of resins for solid-phase synthesis
    • Story S, Aldrich JV. Preparation of protected peptide amides using the Fmoc chemical protocol. Comparision of resins for solid-phase synthesis. Int. J. Peptide Protein Res. 1992; 39: 87-92.
    • (1992) Int. J. Peptide Protein Res. , vol.39 , pp. 87-92
    • Story, S.1    Aldrich, J.V.2
  • 7
    • 0024746193 scopus 로고
    • Synthesis and application of acid labile anchor groups for the synthesis of peptide amides by Fmoc-solid-phase peptide synthesis
    • Breipohl G, Knolle J, Stuber W. Synthesis and application of acid labile anchor groups for the synthesis of peptide amides by Fmoc-solid-phase peptide synthesis. Int. J. Peptide Protein Res. 1989; 34: 262-267.
    • (1989) Int. J. Peptide Protein Res. , vol.34 , pp. 262-267
    • Breipohl, G.1    Knolle, J.2    Stuber, W.3
  • 8
    • 0033597354 scopus 로고    scopus 로고
    • Acetophenone-based linker for solid phase synthesis of secondary amides and sulfonamides on the Multipin™ support
    • Bui CT, Bray AM, Ercole F, Pham Y, Rasoul F, Maeji NJ. Acetophenone-based linker for solid phase synthesis of secondary amides and sulfonamides on the Multipin™ support. Tetrahedron Lett. 1999; 40: 3471-3474.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3471-3474
    • Bui, C.T.1    Bray, A.M.2    Ercole, F.3    Pham, Y.4    Rasoul, F.5    Maeji, N.J.6
  • 9
    • 0002709948 scopus 로고    scopus 로고
    • Intramolecular michael addition of N- And O-centred nucleophiles to tethered acrylates. the role of double-bond geometry in controlling the diastereo-selectivity of cyclisations leading to 2,6-disubstituted tetrahydropyrans and piperidine
    • Banwell MG, Bissett BD, Bui CT, Pham HTT, Simpson GW. Intramolecular michael addition of N-and O-centred nucleophiles to tethered acrylates. The role of double-bond geometry in controlling the diastereo-selectivity of cyclisations leading to 2,6-disubstituted tetrahydropyrans and piperidine. Aust. J. Chem. 1998; 51: 9-18.
    • (1998) Aust. J. Chem. , vol.51 , pp. 9-18
    • Banwell, M.G.1    Bissett, B.D.2    Bui, C.T.3    Pham, H.T.T.4    Simpson, G.W.5
  • 10
    • 0024729231 scopus 로고
    • Synthesis of peptide amides by Fmoc-solid-phase peptide synthesis and acid labile anchor groups
    • Stuber W, Knolle J, Breipohl G. Synthesis of peptide amides by Fmoc-solid-phase peptide synthesis and acid labile anchor groups. Int. J. Peptide Protein Res. 1989; 34: 215-221.
    • (1989) Int. J. Peptide Protein Res. , vol.34 , pp. 215-221
    • Stuber, W.1    Knolle, J.2    Breipohl, G.3
  • 11
    • 0031608249 scopus 로고    scopus 로고
    • Six new photolabile linkers for solid-phase synthesis. 1. Methods of preparation
    • Akerblom EB, Nygren AS, Agback KH. Six new photolabile linkers for solid-phase synthesis. 1. Methods of preparation. Mol. Diversity 1998; 3: 137-148.
    • (1998) Mol. Diversity , vol.3 , pp. 137-148
    • Akerblom, E.B.1    Nygren, A.S.2    Agback, K.H.3
  • 13
    • 0032227722 scopus 로고    scopus 로고
    • Comparative study of reductive aminatlon reaction on 5-(4-formyl-3,5-dimethoxyphenoxy)valeric acid and its monomethoxy-analog using the Multipin™ approach
    • Bui CT, Bray AM, Pham Y, Campbell R, Ercole F, Rasoul F, Maeji NJ. Comparative study of reductive aminatlon reaction on 5-(4-formyl-3,5-dimethoxyphenoxy)valeric acid and its monomethoxy-analog using the Multipin™ approach. Mol. Diversity 1998; 4: 155-163.
    • (1998) Mol. Diversity , vol.4 , pp. 155-163
    • Bui, C.T.1    Bray, A.M.2    Pham, Y.3    Campbell, R.4    Ercole, F.5    Rasoul, F.6    Maeji, N.J.7
  • 15
    • 85006940302 scopus 로고    scopus 로고
    • Novel α-hydroxyethyl-polystyrene, α-chloroethyl-polystyrene and α-amino-oxyethyl-polystyrene linkers on the multipin™ solid support for solid phase organic synthesis
    • in press
    • Bui CT, Maeji NJ, Bray AM. Novel α-hydroxyethyl-polystyrene, α-chloroethyl-polystyrene and α-amino-oxyethyl-polystyrene linkers on the multipin™ solid support for solid phase organic synthesis. Biotechnol. Bioeng. (Combinatorial Chem.); in press.
    • Biotechnol. Bioeng. (Combinatorial Chem.)
    • Bui, C.T.1    Maeji, N.J.2    Bray, A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.