Reactions of benzyl 2-benzyloxycarbonylamino-2-deoxy-3-O-mesyl-.ALPHA.-D-gluco- and -.ALPHA.-D-allopyranoside derivative with iodide.
スポンサーリンク
概要
- 論文の詳細を見る
The reactions of benzyl 4,6-<I>O</I>-benzylidene-2-benzyloxycarbonylamino-2-deoxy-3-<I>O</I>-mesyl-α-D-glucopyranoside (<B>1</B>), its <I>N</I>-methyl derivative (<B>4</B>) and 3-epimer (<B>8</B>) with sodium iodide in DMF were studied. Compound <B>1</B> gave several products including 2,3-alloepimine, <B>4</B> an oxazolidinone and <B>8</B> a 3-iodo derivative.
- 公益社団法人 日本化学会の論文
著者
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Tsuchiya Tsutomu
Institute of Bioorganic Chemistry
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Umezawa Sumio
Institute of Bioorganic Chemistry
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Sano Hiroshi
Institute of Bioorganic Chemistry
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Iimura Seiji
Institute of Bioorganic Chemistry
関連論文
- Reactions of benzyl 2-benzyloxycarbonylamino-2-deoxy-3-O-mesyl-.ALPHA.-D-gluco- and -.ALPHA.-D-allopyranoside derivative with iodide.
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- Structural studies on the cyclic carbamate derivatives of kanamycin A.
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- Reactions of 2-guanidino-1-cyclohexanol with ketals and acetals.
- Synthesis of 5"-deoxy-5"-fluorolividomycin B.
- Synthesis of 2-amino-2,3-dideoxy-L-ribohexose.
- Synthesis of a masked derivative of 3'-deoxydihydrostreptobiosamine, a precursor for the synthesis of 3"-deoxydihydrostreptomycin.
- A synthesis of neamine.
- Synthesis of a lividomycin B analogue, 5-O-[3-O-(2-amino-2-deoxy-.ALPHA.-D-glucopyranosyl)-.BETA.-D-ribofuranosyl]-3'-deoxyparomamine.