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Volumn 45, Issue 52, 2004, Pages 9545-9547

A tandem metathesis-hydrogenation route to dicarba analogues of cystine-containing cyclic peptides

Author keywords

Hydrogenation; Metathesis; Octreotide; Tandem reactions

Indexed keywords

CARBON; CYCLOPEPTIDE; CYSTINE; METAL; OCTREOTIDE; PEPTIDE DERIVATIVE; RESIN;

EID: 9644266915     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.10.165     Document Type: Article
Times cited : (23)

References (27)
  • 5
    • 9644304332 scopus 로고    scopus 로고
    • note
    • 1/2 = 16.9 h and beta emission, 2.11 MeV) are ideal for therapy
  • 16
    • 0034746687 scopus 로고    scopus 로고
    • Intolerance of catalysts to basic functionality has been previously reported. T.M. Trnka, and R.H. Grubbs Acc. Chem. Res. 34 2001 18 29
    • (2001) Acc. Chem. Res. , vol.34 , pp. 18-29
    • Trnka, T.M.1    Grubbs, R.H.2
  • 26
    • 9644290589 scopus 로고    scopus 로고
    • note
    • The unit cell of octreotide contains three individual molecules of the peptide. Only one molecule (Molecule II) possesses the rotomer conformation believed to be associated with biological activity. This molecule was modelled using Insight II with the Discover Minimisation Module (Accelerys: San Diego, C.A.; 1996, Vol. 2002)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.