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methyl (3E,2R)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)pent-3-enoate | 145090-64-8

中文名称
——
中文别名
——
英文名称
methyl (3E,2R)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)pent-3-enoate
英文别名
——
methyl (3E,2R)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)pent-3-enoate化学式
CAS
145090-64-8
化学式
C14H25NO4
mdl
——
分子量
271.357
InChiKey
LZFJSBHGTCZIIX-MYSGNRETSA-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):
    2.75
  • 重原子数:
    19.0
  • 可旋转键数:
    5.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    55.84
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    methyl (3E,2R)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)pent-3-enoate甲酸双氧水臭氧 作用下, 生成 methyl hydrogen (S)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)malonate
    参考文献:
    名称:
    1-(N,N-Diisopropylcarbamoyloxy)-1,3-dimethylallyllithium·(−)-sparteine: stereochemistry of the enantioselective carboxylation and methoxycarbonylation
    摘要:
    The title compound (S)-3/(-)-2, easily available through deprotonation of the racemic O-(2-alkenyl) carbamate under kinetic resolution, undergoes with carbon dioxide or methyl chloroformate predominantly a-substitution with stereoinversion. The absolute configuration of the formed methyl carboxylate is established by chemical correlation, thus correcting our former suggestion3a.
    DOI:
    10.1016/s0040-4020(01)86587-x
  • 作为产物:
    描述:
    氯甲酸甲酯 反应 0.08h, 生成 methyl (3E/Z)-4-methyl-4-(N,N-diisopropylcarbamoyloxy-2-methyl)but-3-enoate 、 methyl (3E,2S)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)pent-3-enoate 、 methyl (3E,2R)-2-methyl-2-(N,N-diisopropylcarbamoyloxy)pent-3-enoate
    参考文献:
    名称:
    1-(N,N-Diisopropylcarbamoyloxy)-1,3-dimethylallyllithium·(−)-sparteine: stereochemistry of the enantioselective carboxylation and methoxycarbonylation
    摘要:
    The title compound (S)-3/(-)-2, easily available through deprotonation of the racemic O-(2-alkenyl) carbamate under kinetic resolution, undergoes with carbon dioxide or methyl chloroformate predominantly a-substitution with stereoinversion. The absolute configuration of the formed methyl carboxylate is established by chemical correlation, thus correcting our former suggestion3a.
    DOI:
    10.1016/s0040-4020(01)86587-x
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