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(E)-N-[2-(2-(1-(phenylsulfonamido)naphthalen-2-yl)vinyl)phenyl]benzenesulfonamide | 1361391-57-2

中文名称
——
中文别名
——
英文名称
(E)-N-[2-(2-(1-(phenylsulfonamido)naphthalen-2-yl)vinyl)phenyl]benzenesulfonamide
英文别名
——
(E)-N-[2-(2-(1-(phenylsulfonamido)naphthalen-2-yl)vinyl)phenyl]benzenesulfonamide化学式
CAS
1361391-57-2
化学式
C30H24N2O4S2
mdl
——
分子量
540.664
InChiKey
OXQLZGBNMLLWCM-LSDHQDQOSA-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):
    6.61
  • 重原子数:
    38.0
  • 可旋转键数:
    8.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    92.34
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    (E)-N-[2-(2-(1-(phenylsulfonamido)naphthalen-2-yl)vinyl)phenyl]benzenesulfonamide碘苯二乙酸四丁基氯化铵 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 6.0h, 以87%的产率得到7,12-bis(phenylsulfonyl)-6b,7,11b,12-tetrahydrobenz[g]indolo[3,2-b]indole
    参考文献:
    名称:
    Intramolecular Oxidative Diamination and Aminohydroxylation of Olefins under Metal-Free Conditions
    摘要:
    A metal-free procedure that is simple to operate and convenient to handle was developed for the facile intramolecular oxidative diamination of olefins using an iodobenzene diacetate oxidant and a halide additive to furnish bisindolines at room temperature. The present reaction is featured by mild conditions, a broad substrate scope, and excellent functional group tolerance. The same protocol was successfully extended to the aminohydroxylation.
    DOI:
    10.1021/ol300166q
  • 作为产物:
    参考文献:
    名称:
    Intramolecular Oxidative Diamination and Aminohydroxylation of Olefins under Metal-Free Conditions
    摘要:
    A metal-free procedure that is simple to operate and convenient to handle was developed for the facile intramolecular oxidative diamination of olefins using an iodobenzene diacetate oxidant and a halide additive to furnish bisindolines at room temperature. The present reaction is featured by mild conditions, a broad substrate scope, and excellent functional group tolerance. The same protocol was successfully extended to the aminohydroxylation.
    DOI:
    10.1021/ol300166q
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