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Volumn 75, Issue 6, 2010, Pages 2111-2114

Solid-phase synthesis of peptide-viologen conjugates

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; HIGH YIELD; ROBUST METHODS; ROOM TEMPERATURE; SOLID PHASE PEPTIDE SYNTHESIS; SOLID PHASE SYNTHESIS; UV SPECTROSCOPY; VIOLOGENS;

EID: 77949835296     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100018f     Document Type: Article
Times cited : (12)

References (28)
  • 25
    • 77949814068 scopus 로고    scopus 로고
    • We have had similar success with peptide conjugation to aminopropyl viologen, and we predict that other aminoalkyl viologens will behave similarly.
    • We have had similar success with peptide conjugation to aminopropyl viologen, and we predict that other aminoalkyl viologens will behave similarly.
  • 26
    • 77949817183 scopus 로고    scopus 로고
    • Compound 3 is dissolved at 25 mM in DMSO at 60 °C, then an equal volume of DMF is added. The DMSO/DIEA. mixture is necessary to solubilize both 3 and DIEA in the same environment.
    • Compound 3 is dissolved at 25 mM in DMSO at 60 °C, then an equal volume of DMF is added. The DMSO/DIEA. mixture is necessary to solubilize both 3 and DIEA in the same environment.
  • 27
    • 77949793546 scopus 로고    scopus 로고
    • One equivalent of DIEA liberates the free amine. The second equivalent is produced from the nucleophilic acyl substitution. We have found that a small (0.4 equiv) excess of DIEA gives consistently better results, but the resin should be rinsed as soon as the reaction is complete.
    • One equivalent of DIEA liberates the free amine. The second equivalent is produced from the nucleophilic acyl substitution. We have found that a small (0.4 equiv) excess of DIEA gives consistently better results, but the resin should be rinsed as soon as the reaction is complete.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.