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Volumn 4, Issue 10, 2013, Pages 1405-1410

Trifluoromethyl derivatives of canonical nucleosides: Synthesis and bioactivity studies

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EID: 84884742726     PISSN: 20402503     EISSN: 20402511     Source Type: Journal    
DOI: 10.1039/c3md00159h     Document Type: Article
Times cited : (30)

References (54)
  • 49
    • 37049108761 scopus 로고
    • 3 group onto the nucleobase can also dramatically destabilize ribose-modified pyrimidine nucleosides. Thus, for example, the trifluoromethylated product of 2′,3′-dideoxy, 2′,3′-didehydrocytidine-where the starting substrate was synthesized by us according to
    • Y. Kobayashi K. Yamamoto T. Asai M. Nakano I. Kumadaki J. Chem. Soc., Perkin Trans. 1 1980 2755
    • (1980) J. Chem. Soc., Perkin Trans. 1 , pp. 2755
    • Kobayashi, Y.1    Yamamoto, K.2    Asai, T.3    Nakano, M.4    Kumadaki, I.5
  • 50
    • 0027369621 scopus 로고
    • did not survive, if not in traces, to the chromatographic purification To the best of our knowledge, this nucleoside has been described in the literature only as the 2′,3′,5′-tri-O-acetyl derivative (see ref. 43) and is unprecedented in its sugar-deprotected form
    • L. De Napoli A. Messere D. Montesarchio G. Piccialli C. Santacroce Nucleosides Nucleotides 1993 12 981
    • (1993) Nucleosides Nucleotides , vol.12 , pp. 981
    • De Napoli, L.1    Messere, A.2    Montesarchio, D.3    Piccialli, G.4    Santacroce, C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.