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(1S,2S,4'R)-1-(4''-azidobutyl)-2-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-4-methylenecyclohexane-1-carbaldehyde | 1256293-40-9

中文名称
——
中文别名
——
英文名称
(1S,2S,4'R)-1-(4''-azidobutyl)-2-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-4-methylenecyclohexane-1-carbaldehyde
英文别名
——
(1S,2S,4'R)-1-(4''-azidobutyl)-2-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-4-methylenecyclohexane-1-carbaldehyde化学式
CAS
1256293-40-9
化学式
C17H27N3O3
mdl
——
分子量
321.42
InChiKey
FVVHTIXNJSBTAE-HLLBOEOZSA-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):
    4.16
  • 重原子数:
    23.0
  • 可旋转键数:
    7.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    84.29
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of a Functionalized 7,6-Bicyclic Spiroimine Ring Fragment of the Spirolides
    摘要:
    The asymmetric synthesis of a functionalized 7,6-spiroimine related to the spirolides is described. Intermolecular Diels-Alder cycloaddition of a chiral trisubstituted dienophile and Danishefsky's diene enabled simultaneous installation of the C7 and C29 stereocenters. Further transformations and late-stage aza-Wittig cyclization afforded the spiroimine in good yield. During this study, an unprecedented 14-membered dialdimine was also obtained.
    DOI:
    10.1021/ol102525w
  • 作为产物:
    描述:
    (1S,2S,4'R)-1-(4''-(p-methylbenzenesulfonyloxy)butyl)-2-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-4-methylenecyclohexane-1-carbaldehyde 在 sodium azide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 8.0h, 以73%的产率得到(1S,2S,4'R)-1-(4''-azidobutyl)-2-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-4-methylenecyclohexane-1-carbaldehyde
    参考文献:
    名称:
    Synthesis of a Functionalized 7,6-Bicyclic Spiroimine Ring Fragment of the Spirolides
    摘要:
    The asymmetric synthesis of a functionalized 7,6-spiroimine related to the spirolides is described. Intermolecular Diels-Alder cycloaddition of a chiral trisubstituted dienophile and Danishefsky's diene enabled simultaneous installation of the C7 and C29 stereocenters. Further transformations and late-stage aza-Wittig cyclization afforded the spiroimine in good yield. During this study, an unprecedented 14-membered dialdimine was also obtained.
    DOI:
    10.1021/ol102525w
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