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(1S)-1-[(2S,3S,5R,6R)-3-[(1S)-1-hydroxybut-3-enyl]-5,6-dimethoxy-5,6-dimethyl-1,4-dioxan-2-yl]ethane-1,2-diol | 930793-13-8

中文名称
——
中文别名
——
英文名称
(1S)-1-[(2S,3S,5R,6R)-3-[(1S)-1-hydroxybut-3-enyl]-5,6-dimethoxy-5,6-dimethyl-1,4-dioxan-2-yl]ethane-1,2-diol
英文别名
——
(1S)-1-[(2S,3S,5R,6R)-3-[(1S)-1-hydroxybut-3-enyl]-5,6-dimethoxy-5,6-dimethyl-1,4-dioxan-2-yl]ethane-1,2-diol化学式
CAS
930793-13-8
化学式
C14H26O7
mdl
——
分子量
306.356
InChiKey
VUMHTNDNGWQJBP-SNIKSBKOSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.6
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    97.6
  • 氢给体数:
    3
  • 氢受体数:
    7

反应信息

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文献信息

  • Enantiospecific Synthesis of Pseudoacarviosin as a Potential Antidiabetic Agent
    作者:Tony K. M. Shing、Hau M. Cheng、Wai F. Wong、Connie S. K. Kwong、Jianmei Li、Clara B. S. Lau、Po Sing Leung、Christopher H. K. Cheng
    DOI:10.1021/ol8010503
    日期:2008.7.17
    A pseudo-1,4'- N-linked disaccharide, pseudoacarviosin 5, was constructed via a key palladium-catalyzed coupling reaction of pseudoglycosyl chloride 8 (prepared from d-glucose via a novel direct intramolecular aldol addition in 12 steps) and pseudo-4-amino-4,6-dideoxy-alpha- d-glucose 9 (prepared from l-arabinose via an unusual trans-fused isoxazolidine-selective intramolecular nitrone-alkene cycloaddition
    伪1,4'-N-连接的二糖伪拟紫薇香素5是通过在关键的催化的拟糖基8的偶联反应(由d-葡萄糖通过12步新颖的直接分子内羟醛加成反应制得的)和拟糖基构成的。 4-基-4,6-二脱氧-α-d-葡萄糖9(由A-阿拉伯糖通过不寻常的反式融合的异恶唑烷选择性分子内氮烯-烯烃环加成反应制备而成,共11步)。伪胡萝卜素5已被证明是α-葡糖苷酶的有效抑制剂,尤其是与血糖控制有关的肠粘膜酶蔗糖酶和葡糖淀粉酶
  • Carbocyclization of Carbohydrates: Diastereoselective Synthesis of (+)-Gabosine F, (−)-Gabosine O, and (+)-4-<i>epi</i>-Gabosine O
    作者:Tony K. M. Shing、King H. So、Wun S. Kwok
    DOI:10.1021/ol902071e
    日期:2009.11.5
    Exploitation of silica gel/chloramine T mediated intramolecular nitrile oxide-alkene cycloaddition (INOC) of sugar-derived oximes to carbocycles furnished the first synthesis of gabosine F from L-arabinose in 12 steps with 23% overall yield, thereby confirming it absolute configuration. Similarly, efficient syntheses of gabosine O and 4-epi-gabosine O were accomplished from D-Mannose in 9 and 11 steps with 41% and 38% overall yields, respectively, involving INOC, regioselective dehydration, and diastereciselective hydrogenation as the key steps.
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