(1S)-2t,6t-bis-benzyloxycarbonylamino-4c-(2-benzyloxycarbonylamino-α-D-ribo-2,3-dideoxy-hexopyranosyloxy)-cyclohexane-1r,3t-diol | 73488-20-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1S)-2t,6t-bis-benzyloxycarbonylamino-4c-(2-benzyloxycarbonylamino-α-D-ribo-2,3-dideoxy-hexopyranosyloxy)-cyclohexane-1r,3t-diol
• 英文别名: 1L-1,4-bis-benzyloxycarbonylamino-O⁶-(2-benzyloxycarbonylamino-α-D-ribo-2,3-dideoxy-hexopyranosyl)-1,2,4-trideoxy-muco-inositol
• CAS: 73488-20-7
• 化学式: C₃₆H₄₃N₃O₁₂
• 分子量: 709.75
• InChiKey: YTYQEBFOUUBHOK-DWODQLMBSA-N

反应信息

• 作为反应物：
  描述：

  (1S)-2t,6t-bis-benzyloxycarbonylamino-4c-(2-benzyloxycarbonylamino-α-D-ribo-2,3-dideoxy-hexopyranosyloxy)-cyclohexane-1r,3t-diol 在 barium dihydroxide 、 sodium azide 、 barium(II) oxide 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 (3aR)-7c-(6-azido-2-benzyloxycarbonylamino-α-D-ribo-2,3,6-trideoxy-hexopyranosyloxy)-6t-benzyloxycarbonylamino-4c-hydroxy-3-methyl-(3ar,7ac)-hexahydro-benzooxazol-2-one
  参考文献：
  名称：

  Syntheses of sporaricin analogues, 2-deoxy-4-N-glycyl-6-O-(.ALPHA.-nebrosaminyl)fortamine and its 3-de-O-methyl compound.

  摘要：

  2-Deoxy-4-N-glycyl-6-O-(α-nebrosaminyl)fortamine (21) and 3-de-O-methyl-2-deoxy-4-N-glycyl-6-O-(α-nebrosaminyl)fortamine (27) were prepared starting from lividamine. The syntheses include four key steps, that is, transformation of 2-deoxystreptamine moiety of lividamine to 4-N, 3-O-didemethyl-2-deoxyfortamine, selective 4-N-methylation of the new aminocyclitol moiety, selective attachment of a glycyl residue to the methylamino group at C-4 and selective amination at C-6'.

  DOI：

  10.7164/antibiotics.32.1137