N-(2,2-diethoxycarbonylvinyl)-2,3,4,6-tetra-O-mesyl-β-D-glucopyranosylamine | 173595-48-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: N-(2,2-diethoxycarbonylvinyl)-2,3,4,6-tetra-O-mesyl-β-D-glucopyranosylamine
• 英文别名: diethyl 2-[[[(2R,3R,4S,5R,6R)-3,4,5-tris(methylsulfonyloxy)-6-(methylsulfonyloxymethyl)oxan-2-yl]amino]methylidene]propanedioate
• CAS: 173595-48-7
• 化学式: C₁₈H₃₁NO₁₇S₄
• 分子量: 661.705
• InChiKey: AOLFBMVLNIIGMQ-IBEHDNSVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.6
• 重原子数：
  40
• 可旋转键数：
  17
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  281
• 氢给体数：
  1
• 氢受体数：
  18

反应信息

• 作为反应物：
  描述：

  N-(2,2-diethoxycarbonylvinyl)-2,3,4,6-tetra-O-mesyl-β-D-glucopyranosylamine 在 sodium methylate 、 氢气 、 氯 作用下， 以 六甲基磷酰三胺 、 二氯甲烷 、 水 、 溶剂黄146 为溶剂， 反应 2.0h， 生成 Methanesulfonic acid (2S,3R,4S,5R,6R)-2,6-dihydroxy-3,5-bis-methanesulfonyloxy-azepan-4-yl ester
  参考文献：
  名称：

  Efficient synthesis of seven-membered iminocyclitols from glycosylenamines

  摘要：

  Seven membered iminocyclitols are synthesized in four steps from easily available glycosylenamines (D-gluco, D-galacto, and D-manno configurations) through 1,6-aza-anhydrosugar derivatives. These intermediates are transformed into 2-hydroxy- and 2-unsubstituted azepanes depending on the reactants used for the cleavage of the C1-O bond. The overall yields are high. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(99)00649-8
• 作为产物：
  描述：

  N-(2,2-diethoxycarbonylvinyl)-β-D-glucopyranosylamine 、 甲基磺酰氯 在 吡啶 作用下， 反应 3.0h， 以98%的产率得到N-(2,2-diethoxycarbonylvinyl)-2,3,4,6-tetra-O-mesyl-β-D-glucopyranosylamine
  参考文献：
  名称：

  An easy route to seven-membered iminocyclitols from aldohexopyranosyl enamines

  摘要：

  A new stereocontrolled and high yielding synthesis of biologically active polyhydroxyperhydroazelpines is reported starting from easily available glycosylenamines (D-gluco, D-manno, and D-galacto configurations), which are transformed into 1,6-azaanhydropyranose derivatives. O- and N-Deprotection of the latter, followed by reduction with sodium cyanoborohydride, gives the target chiral iminocyclitols. The method is based on the capacity of the dialkoxycarbonylvinyl group to stabilize an amide ion, and the only limitation is the necessity for the starting glycosylenamine to have beta-D-configuration. The inhibitory activity of several intermediate iminocyclitols and aldopyranosylenamines on different alpha- and beta-glycosidases is also reported. (C) 2002 Published by Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(02)00377-4

文献信息

• Rearrangements of O-protected glycosylenamines. A new and efficient route for the synthesis of O-protected 4-aminoaldoses
  作者：M Angeles Pradera、David Olano、José Fuentes

  DOI：10.1016/0040-4039(95)01737-3

  日期：1995.11

  O-Protected 4-deoxy -4-diethoxycarbonylaminoaldoses with D-galacto. I.-arabino and I-lyxo contigurations (3) are prepared by a nucleophilic rearrangement of easily available glycosylamine derivatives

  O-保护的带有D-半乳糖的4-脱氧-4-二乙氧基羰基氨基醛糖。余。阿拉伯糖和我-lyxo contigurations（3）由容易获得的糖基胺衍生物的亲核重排制备