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Methyl 3-benzyl-7,7-dicyano-5-methylidene-2-oxooxonane-3-carboxylate | 1198581-75-7

中文名称
——
中文别名
——
英文名称
Methyl 3-benzyl-7,7-dicyano-5-methylidene-2-oxooxonane-3-carboxylate
英文别名
methyl 3-benzyl-7,7-dicyano-5-methylidene-2-oxooxonane-3-carboxylate
Methyl 3-benzyl-7,7-dicyano-5-methylidene-2-oxooxonane-3-carboxylate化学式
CAS
1198581-75-7
化学式
C20H20N2O4
mdl
——
分子量
352.39
InChiKey
IPTDRRDNZXMVBR-UHFFFAOYSA-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):
    2.6
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    100
  • 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:
    α-methoxycarbonyl-α-benzyl-γ-methylidene-δ-valerolactone环丙烷-1,1-二腈allyl(cyclopentadiene)palladium(II) 、 N,N-diethylbenzo[d][1,3,2]benzodioxaphosphepin-6-amine 作用下, 以 甲苯 为溶剂, 反应 48.08h, 以73%的产率得到Methyl 3-benzyl-7,7-dicyano-5-methylidene-2-oxooxonane-3-carboxylate
    参考文献:
    名称:
    Palladium-Catalyzed Decarboxylative [4 + 3] Cyclization of γ-Methylidene-δ-valerolactones with 1,1-Dicyanocyclopropanes
    摘要:
    A palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes has been developed to produce cycloheptane derivatives in a convergent manner. This method can be applied to the synthesis of azepanes by reacting with aziridines, and their asymmetric variants have also been described. In addition, selective ring-expansion reactions can be achieved for certain gamma-methylidene-delta-valerolactones to give nondecarboxylated nine-membered lactones.
    DOI:
    10.1021/ol902326s
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文献信息

  • Palladium-Catalyzed Decarboxylative [4 + 3] Cyclization of γ-Methylidene-δ-valerolactones with 1,1-Dicyanocyclopropanes
    作者:Ryo Shintani、Masataka Murakami、Takaoki Tsuji、Hideyuki Tanno、Tamio Hayashi
    DOI:10.1021/ol902326s
    日期:2009.12.17
    A palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes has been developed to produce cycloheptane derivatives in a convergent manner. This method can be applied to the synthesis of azepanes by reacting with aziridines, and their asymmetric variants have also been described. In addition, selective ring-expansion reactions can be achieved for certain gamma-methylidene-delta-valerolactones to give nondecarboxylated nine-membered lactones.
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