Tubercidin. Its Conversion into 5′-Deoxytubercidin
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概要
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Tubercidin (I) was converted into 5′-deoxytubercidin (IV). Mesylation of 2′,3′-<I>O</I>-isopropylidenetubercidin (IX) afforded-2′,3′-<I>O</I>-isopropylidene-5′-<I>O</I>-mesyltubercidin (XVIII), which <I>in situ</I> was treated with benzoyl chloride. The product, <I>N</I><SUP>6</SUP>,<I>N</I><SUP>6</SUP>-dibenzoyl-2′,3′-<I>O</I>-isopropylidene-5′-<I>O</I>-mesyltubercidin (XXII), was converted into <I>N</I><SUP>6</SUP>,<I>N</I><SUP>6</SUP>-dibenzoyl-5′-deoxy-5′-iodo-2′,3′-<I>O</I>-isopropylidenetubercidin (XXIV). Catalytic hydrogenation of XXIV afforded <I>N</I><SUP>6</SUP>-benzoyl-5′-deoxy-2′,3′-<I>O</I>-isopropylidenetubercidin (XXVII). 5′-Deoxytubercidin (IV) was obtained on debenzoylation and deacetonation of XXVII.
- 公益社団法人 日本化学会の論文
著者
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Anzai Kentaro
The Institute of Physical and Chemical Research
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Matsui Masanao
The Institute of Physical and Chemical Research
関連論文
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