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  • Biochemistry and Biotechnology  (2)
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 61 (1998), S. 89-92 
    ISSN: 0006-3592
    Schlagwort(e): solid phase chemistry ; Merrifield linker ; Suzuki coupling ; Stille coupling ; Pd(0) mediated C-S bond formation ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: We report the convenient generation of chloromethylated polystyrene surfaces (Merrifield linker)3 on SynPhase™ crowns. It was demonstrated that these novel surfaces can be successfully employed for peptide chemistry as well as Pd(0) mediated cross-couplings. © 1998 John Wiley & Sons, Inc. Biotechnol Bioeng (Comb Chem) 61:89-92, 1998.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Peptide Science 1 (1995), S. 80-87 
    ISSN: 1075-2617
    Schlagwort(e): Multiple synthesis ; optimizing peptide synthesis ; N-terminal asparagine ; BOP ; HATU ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The multipin method of peptide synthesis is demonstrated as a potent methodological tool, where large numbers of comparative studies can be performed concurrently. Two studies are presented. In each study, the test peptides were simultaneously synthesized, and the products examined by high throughput ion spray mass spectrometry and reverse-phase HPLC. In the first study, comprising 24 experiments, peptides 1 (AELFSTHYLAFKEDYSQ-NH2) and 2 (LKDFRVYFREGRDQLWKGPG-NH2) were prepared using Fmoc-Axx/BOP/HOBt/NMM (100: 100: 100: 150 mM) and Fmoc-Axx/HATU/HOAt/NMM (100: 100: 100: 150 mM) with 60.90 and 120 min coupling times. The two reagent combinations were found to give comparable results. The second study compared the N-terminal coupling of Fmoc-Asn-OH, Fmoc-Asn(Mbh)-OH, Fmoc-Asn(Mtt)-OH, Fmoc-Asn(Tmob)-OH and Fmoc-Asn(Trt)-OH in the synthesis of seven test peptides: 3, NVQAAIDYIG-cyclo(Kp); 4, NTVQAAIDYIG-cyclo(KF); 5, NRVYVHPFNL; 6, NRVYVHPFHL: 7, NEAYVHDAPVRSLN: 8, NQLVVPSEGLYLIYSQVLFK. 9, NPNANPNANPNA. A total of 33 experiments were performed. Peptides 3 and 4 were selected to highlight the effect of steric bulk of each Asn derivative on coupling efficiency. Reagent efficiency, as measured by target peptide purity, was as follows: Fmoc-Asn(Tmob)-OH 〉 Fmoc-Asn-OH 〉 Fmoc-Asn(Mtt)-OH = Fmoc-Asn(Trt)-OH 〉 Fmoc-Asn(Mbh)-OH.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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