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(2R)-7-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-8,8-dimethyl-2-(tri-isopropylsilyloxy)-dec-9-ene-4,6-dione | 1334485-07-2

中文名称
——
中文别名
——
英文名称
(2R)-7-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-8,8-dimethyl-2-(tri-isopropylsilyloxy)-dec-9-ene-4,6-dione
英文别名
(2R)-7-(2,2-dimethyl-6-oxo-1,3-dioxin-4-yl)-8,8-dimethyl-2-tri(propan-2-yl)silyloxydec-9-ene-4,6-dione
(2R)-7-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-8,8-dimethyl-2-(tri-isopropylsilyloxy)-dec-9-ene-4,6-dione化学式
CAS
1334485-07-2
化学式
C27H46O6Si
mdl
——
分子量
494.744
InChiKey
QJLLSOFURQGSMD-VGOKPJQXSA-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):
    6.51
  • 重原子数:
    34
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    78.9
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    (5R)-3-methylbut-2-enyl 2-(2-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)acetyl)-3-oxo-5-(tri-isopropylsilyloxy)hexanoate四(三苯基膦)钯caesium carbonate 作用下, 以 四氢呋喃 为溶剂, 反应 18.0h, 以10%的产率得到(2R)-7-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-8,8-dimethyl-2-(tri-isopropylsilyloxy)-dec-9-ene-4,6-dione
    参考文献:
    名称:
    Biomimetic Total Synthesis of Angelicoin A and B via a Palladium-Catalyzed Decarboxylative Prenylation-Aromatization Sequence
    摘要:
    Five-step total syntheses of angelicoin A and B from 2,2,6-trimethyl-4-dioxinone are reported using late stage biomimetic aromatization reactions via diketo-dioxinones as intermediates. In addition, with angelicoin A, this aromatization was coupled with a palladium-catalyzed decarboxylative prenylation in a one-pot sequence as the key step.
    DOI:
    10.1021/ol202320m
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文献信息

  • Biomimetic Total Synthesis of Angelicoin A and B via a Palladium-Catalyzed Decarboxylative Prenylation-Aromatization Sequence
    作者:Katie Anderson、Frederick Calo、Toni Pfaffeneder、Andrew J. P. White、Anthony G. M. Barrett
    DOI:10.1021/ol202320m
    日期:2011.11.4
    Five-step total syntheses of angelicoin A and B from 2,2,6-trimethyl-4-dioxinone are reported using late stage biomimetic aromatization reactions via diketo-dioxinones as intermediates. In addition, with angelicoin A, this aromatization was coupled with a palladium-catalyzed decarboxylative prenylation in a one-pot sequence as the key step.
  • Total Syntheses of Angelicoin A, Hericenone J, and Hericenol A via Migratory Prenyl- and Geranylation–Aromatization Sequences
    作者:Jens Cordes、Frederick Calo、Katie Anderson、Toni Pfaffeneder、Sylvain Laclef、Andrew J. P. White、Anthony G. M. Barrett
    DOI:10.1021/jo202354j
    日期:2012.1.6
    A five-step synthesis of the natural product angelicoin A using a late stage highly regioselective palladium(0)-catalyzed decarboxylative prenyl migration and aromatization sequence as the key step is reported. The method was extended with geranyl migration in eight-step total syntheses of hericenone J and hericenol A from geraniol.
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