Studies toward Stable Analogues of Guanofosfocins. Synthesis of the Protected Derivative of 8-(5a-Carba-α-D-mannopyranosyloxy)purine Nucleoside

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著者

    • HOSOGAI Naoya
    • Faculty of Education and Human Sciences, Yokohama National University

抄録

As a preliminary study directed towards the synthesis of a stable analogue of the guanofosfocins, a methylene analogue of the endocyclic oxygen atom in the mannose moiety, was designed. The construction of the pseudo-α-mannosyl linkage at the 8-position of the purine nucleoside was accomplished by the regioselective ring-opening substitution of the 1,2-<I>O</I>-cyclic sulfate derivative of 5a-carba-mannopyranose.

収録刊行物

  • Chemistry letters  

    Chemistry letters 36(1), 36-37, 2007-01-05 

    The Chemical Society of Japan

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各種コード

  • NII論文ID(NAID)
    10018662625
  • NII書誌ID(NCID)
    AA00603318
  • 本文言語コード
    ENG
  • 資料種別
    SHO
  • ISSN
    03667022
  • データ提供元
    CJP書誌  J-STAGE 
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