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Volumn 132, Issue 3, 2011, Pages 166-174

Regioselective synthesis of 5-trifluoromethyl-1,2,3-triazole nucleoside analogues via TBS-directed 1,3-dipolar cycloaddition reaction

Author keywords

1,3 Dipolar cycloaddition; Nucleoside analogues; Regioselective synthesis; Triazole; Trifluoromethyl group

Indexed keywords


EID: 79952440820     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2010.12.012     Document Type: Article
Times cited : (14)

References (51)
  • 1
    • 77949893001 scopus 로고    scopus 로고
    • For reviews on the chemistry synthesis and biological activity of nucleoside analogues see: A. Mieczkowski, and L.A. Agrofoglio Modif. Nucleos. 2008 393 424
    • (2008) Modif. Nucleos. , pp. 393-424
    • Mieczkowski, A.1    Agrofoglio, L.A.2
  • 10
    • 70349144073 scopus 로고    scopus 로고
    • For reviews of triazolo nucleoside analogues and heterocyclic-sugar nucleoside analogues, see: F. Amblard, J.H. Cho, and R.F. Schinazi Chem. Rev. 109 2009 4207 4220
    • (2009) Chem. Rev. , vol.109 , pp. 4207-4220
    • Amblard, F.1    Cho, J.H.2    Schinazi, R.F.3
  • 38
    • 79952441326 scopus 로고    scopus 로고
    • note
    • 3 group attached.
  • 48
    • 79952441709 scopus 로고    scopus 로고
    • The crystal structure has been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number CCDC 787398
    • The crystal structure has been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number CCDC 787398.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.