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4-((2R,3R)-3-(2-((R)-3,3-dimethyloxiran-2-yl)ethyl)-3-methyloxiran-2-yl)but-1-en-2-yl trifluoromethanesulfonate | 1221900-32-8

中文名称
——
中文别名
——
英文名称
4-((2R,3R)-3-(2-((R)-3,3-dimethyloxiran-2-yl)ethyl)-3-methyloxiran-2-yl)but-1-en-2-yl trifluoromethanesulfonate
英文别名
——
4-((2R,3R)-3-(2-((R)-3,3-dimethyloxiran-2-yl)ethyl)-3-methyloxiran-2-yl)but-1-en-2-yl trifluoromethanesulfonate化学式
CAS
1221900-32-8
化学式
C14H21F3O5S
mdl
——
分子量
358.379
InChiKey
NNFTXLYAQLBHIW-NQBHXWOUSA-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):
    3.26
  • 重原子数:
    23.0
  • 可旋转键数:
    8.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    68.43
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    4-((2R,3R)-3-(2-((R)-3,3-dimethyloxiran-2-yl)ethyl)-3-methyloxiran-2-yl)but-1-en-2-yl trifluoromethanesulfonate(三甲基硅基)甲基氯化镁四(三苯基膦)钯 作用下, 以 四氢呋喃乙醚 为溶剂, 以85%的产率得到[4-[(2R,3R)-3-[2-[(2R)-3,3-dimethyloxiran-2-yl]ethyl]-3-methyloxiran-2-yl]-2-methylidenebutyl]-trimethylsilane
    参考文献:
    名称:
    Biomimetic Syntheses from Squalene-Like Precursors: Synthesis of ent-Abudinol B and Reassessment of the Structure of Muzitone
    摘要:
    We achieved the stereoselective syntheses of two different structural patterns corresponding to the enantiomers of the marine natural products abudinol B and muzitone, by developing two-directional tandem biomimetic cyclizations of polyepoxides of squalene analogues in which one alkene was functionalized as an enolsilane. In the course of this work, we demonstrated that the structure of muzitone was misassigned.
    DOI:
    10.1021/ja1006806
  • 作为产物:
    描述:
    N-苯基双(三氟甲烷磺酰)亚胺 、 在 双(三甲基硅烷基)氨基钾 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 3.0h, 以70%的产率得到4-((2R,3R)-3-(2-((R)-3,3-dimethyloxiran-2-yl)ethyl)-3-methyloxiran-2-yl)but-1-en-2-yl trifluoromethanesulfonate
    参考文献:
    名称:
    Biomimetic Syntheses from Squalene-Like Precursors: Synthesis of ent-Abudinol B and Reassessment of the Structure of Muzitone
    摘要:
    We achieved the stereoselective syntheses of two different structural patterns corresponding to the enantiomers of the marine natural products abudinol B and muzitone, by developing two-directional tandem biomimetic cyclizations of polyepoxides of squalene analogues in which one alkene was functionalized as an enolsilane. In the course of this work, we demonstrated that the structure of muzitone was misassigned.
    DOI:
    10.1021/ja1006806
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