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3-cyano-7-methoxymethoxy-1(3H)isobenzo-furanone | 113232-79-4

中文名称
——
中文别名
——
英文名称
3-cyano-7-methoxymethoxy-1(3H)isobenzo-furanone
英文别名
4-(methoxymethoxy)-3-oxo-1H-2-benzofuran-1-carbonitrile
3-cyano-7-methoxymethoxy-1(3H)isobenzo-furanone化学式
CAS
113232-79-4
化学式
C11H9NO4
mdl
——
分子量
219.197
InChiKey
GHTOHXPDBZJKSI-UHFFFAOYSA-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):
    1.3
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    68.6
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Studies towards the total synthesis of mumbaistatin: synthesis of highly substituted benzophenone and anthraquinone building blocks
    摘要:
    Model compounds and building blocks for a planned total synthesis of the highly potent glucose-6-phosphate (G6P) translocase inhibitor mumbaistatin (1) and structural analogs were elaborated: compound 1 represents a lead structure in the development of potential new antidiabetic drugs. With the model substrate 20 it was demonstrated that highly functionalized, tetra-ortho-substituted benzophenones can be prepared by nucleophilic addition of an aryllithium-building block to a benzaldehyde followed by oxidation. For compound 37, a potential precursor of the anthraquinone part of mumbaistatin, various approaches via aryne/phthalide annulations were developed and evaluated. The required functionalized arenes were prepared exploiting, among others, regioselective bromination and ortho-lithiation reactions. Coupling reactions of the anthracene-carbaldehyde 44 derived from 37 with various metalated arenes proved to be unexpectedly difficult and failed so far. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(03)00427-7
  • 作为产物:
    参考文献:
    名称:
    Okazaki, Kousuke; Nomura, Keiichi; Yoshii, Eiichi, Synthetic Communications, 1987, vol. 17, # 9, p. 1021 - 1028
    摘要:
    DOI:
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文献信息

  • Carbene-Catalyzed Formal [5 + 5] Reaction for Coumarin Construction and Total Synthesis of Defucogilvocarcins
    作者:Xuan Huang、Tingshun Zhu、Zhijian Huang、Yuexia Zhang、Zhichao Jin、Giuseppe Zanoni、Yonggui Robin Chi
    DOI:10.1021/acs.orglett.7b03102
    日期:2017.11.17
    An N-heterocyclic carbene-catalyzed formal [5 + 5] reaction between enals and furanones that generates multisubstituted coumarins in a single step is reported. Five atoms in each of the substrates are involved in this catalytic process to form a benzene and a lactone ring. The power of the method is further demonstrated in metal-free total syntheses of several natural products (defucogilvocarcins M
    据报道,在烯醛和呋喃酮之间的N杂环卡宾催化的正式[5 + 5]反应可在一个步骤中生成多取代的香豆素。每个底物中的五个原子参与该催化过程以形成苯和内酯环。该方法的功效在以香豆素为关键结构基序的几种天然产物(去甲福尔霉素M,E和V)的无属全合成中得到了进一步证明。
  • OKAZAKI, KOUSUKE;NOMURA, KEIICHI;YOSHII, EIICHI, SYNTH. COMMUN., 17,(1987) N 9, 1021-1027
    作者:OKAZAKI, KOUSUKE、NOMURA, KEIICHI、YOSHII, EIICHI
    DOI:——
    日期:——
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