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Volumn 75, Issue 10, 2010, Pages 3283-3293

Further studies toward the stereocontrolled synthesis of silicon-containing peptide mimics

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTATES; DIPEPTIDE; DIPHENYLSILANE; HUMAN ISLETS; HUMAN NEUTROPHIL ELASTASE; PEPTIDE MIMICS; POTENTIAL INHIBITORS; PROTEASE INHIBITOR; SIDE CHAINS; STEREOCONTROLLED SYNTHESIS; SULFINIMINES; SYNTHETIC METHODOLOGY;

EID: 77952498164     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100301n     Document Type: Article
Times cited : (39)

References (69)
  • 1
    • 0000120505 scopus 로고
    • Bioorganosilicon chemistry
    • Patai, S., Rappoport, Z., Eds.; John Wiley & Sons: New York, Chapter 18
    • Tacke, R.; Linoh, H. Bioorganosilicon Chemistry. In The Chemistry of Organic Silicon Compounds; Patai, S., Rappoport, Z., Eds.; John Wiley & Sons: New York, 1989; Vol. 1, Chapter 18, pp 1143-1207.
    • (1989) The Chemistry of Organic Silicon Compounds , vol.1 , pp. 1143-1207
    • Tacke, R.1    Linoh, H.2
  • 22
    • 33751158672 scopus 로고
    • For some examples of peptide isosteres, see
    • For some examples of peptide isosteres, see: Wipf, P.; Fritch, P. C. J. Org. Chem. 1994, 59, 4875
    • (1994) J. Org. Chem. , vol.59 , pp. 4875
    • Wipf, P.1    Fritch, P.C.2
  • 53
  • 69
    • 77952484215 scopus 로고    scopus 로고
    • note
    • Attempts to cleave the Si-Ph bonds upon treatment with triflic acid as for the diphenylsilane 53, followed by transformation to the difluoride, were not successful, possibly because of sensitivity of the terminal Boc group to these highly acidic conditions. Nevertheless, we are currently investigating the fibrillating properties of the diphenylsilane analogue of this hexapeptide, as well as its ability to perhaps inhibit the fibrillation process of the parent peptide.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.