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(E)-(R)-5-Iodo-2,4-dimethyl-pent-4-enal | 321995-07-7

中文名称
——
中文别名
——
英文名称
(E)-(R)-5-Iodo-2,4-dimethyl-pent-4-enal
英文别名
(E,2R)-5-iodo-2,4-dimethylpent-4-enal
(E)-(R)-5-Iodo-2,4-dimethyl-pent-4-enal化学式
CAS
321995-07-7
化学式
C7H11IO
mdl
——
分子量
238.068
InChiKey
DRZQHAAFHLVMLP-PTYLAXBQSA-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):
    2.5
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    (E)-(R)-5-Iodo-2,4-dimethyl-pent-4-enal18-冠醚-6四溴化碳potassium tert-butylate双(三甲基硅烷基)氨基钾二异丁基氢化铝三苯基膦 作用下, 以 四氢呋喃二氯甲烷甲苯乙腈 为溶剂, 反应 1.33h, 生成 (2S,6S)-2-((1E,3Z,7E)-(R)-8-Iodo-3,5,7-trimethyl-octa-1,3,7-trienyl)-6-isopropoxy-3,6-dihydro-2H-pyran
    参考文献:
    名称:
    The First Total Synthesis of (+)-Ratjadone
    摘要:
    The first total synthesis of ratjadone was achieved using a highly convergent approach joining three subunits together with a Wittig olefination and a selective Heck reaction as the pivotal steps. Besides establishing a robust and reliable route for the synthesis of this orphan ligand, the configuration of unknown stereocenters could also be determined. This synthesis not only provides an additional access to a biologically important compound but also enables the synthesis of structural analogues for biological target identification.
    DOI:
    10.1021/jo005768g
  • 作为产物:
    参考文献:
    名称:
    The First Total Synthesis of (+)-Ratjadone
    摘要:
    The first total synthesis of ratjadone was achieved using a highly convergent approach joining three subunits together with a Wittig olefination and a selective Heck reaction as the pivotal steps. Besides establishing a robust and reliable route for the synthesis of this orphan ligand, the configuration of unknown stereocenters could also be determined. This synthesis not only provides an additional access to a biologically important compound but also enables the synthesis of structural analogues for biological target identification.
    DOI:
    10.1021/jo005768g
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文献信息

  • Total Synthesis of (+)-Ratjadone
    作者:Mathias Christmann、Ulhas Bhatt、Monika Quitschalle、Eckhard Claus、Markus Kalesse
    DOI:10.1002/1521-3773(20001201)39:23<4364::aid-anie4364>3.0.co;2-g
    日期:2000.12.1
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