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(Z)-N,N-diisopropyl-3-(trimethylstannyl)-2-heptenamide | 363138-71-0

中文名称
——
中文别名
——
英文名称
(Z)-N,N-diisopropyl-3-(trimethylstannyl)-2-heptenamide
英文别名
(Z)-N,N-di(propan-2-yl)-3-trimethylstannylhept-2-enamide
(Z)-N,N-diisopropyl-3-(trimethylstannyl)-2-heptenamide化学式
CAS
363138-71-0
化学式
C16H33NOSn
mdl
——
分子量
374.154
InChiKey
UFRJHGBLPVTMDZ-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):
    4.63
  • 重原子数:
    19
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    (Z)-N,N-diisopropyl-3-(trimethylstannyl)-2-heptenamide溶剂黄146 作用下, 生成 N,N-diisopropyl-2-heptenamide
    参考文献:
    名称:
    Carbamoylstannation of Terminal Alkynes with Carbamoylstannanes:  Catalyst-Dependent Regiochemical Reversal
    摘要:
    Rh(acac)(CO)(2) catalyzes addition of (N,N-diisopropylcarbamoyl)trimethylstannane to terminal alkynes to give (Z)-beta-stannyl-alpha,beta-unsaturated amides with terminal attachment of the amide group, while the use of Ni(COd)(2) results in the reversal of the regioselectivity. A mechanism initiated by the oxidative addition of the carbamoylstannane was proposed on the basis of the isolation of (trimethylstannyl)(N,N-diisopropylcarbamoyl)[1,2-bis(dimethylphosphtno)ethane]pallidium.
    DOI:
    10.1021/om000423+
  • 作为产物:
    描述:
    trimethyl-N,N-di-isopropylcarbamoylstannane1-己炔tris(triphenylphosphine)ruthenium(II) chloride 作用下, 以0%的产率得到(Z)-N,N-diisopropyl-3-(trimethylstannyl)-2-heptenamide
    参考文献:
    名称:
    Carbamoylstannation of Terminal Alkynes with Carbamoylstannanes:  Catalyst-Dependent Regiochemical Reversal
    摘要:
    Rh(acac)(CO)(2) catalyzes addition of (N,N-diisopropylcarbamoyl)trimethylstannane to terminal alkynes to give (Z)-beta-stannyl-alpha,beta-unsaturated amides with terminal attachment of the amide group, while the use of Ni(COd)(2) results in the reversal of the regioselectivity. A mechanism initiated by the oxidative addition of the carbamoylstannane was proposed on the basis of the isolation of (trimethylstannyl)(N,N-diisopropylcarbamoyl)[1,2-bis(dimethylphosphtno)ethane]pallidium.
    DOI:
    10.1021/om000423+
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