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| 1313049-05-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1313049-05-6
化学式
C14H14Cl2N2O2S
mdl
——
分子量
345.249
InChiKey
HHGHALGQEOAMNS-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    3-(hex-1-yn-1-yl)oxazolidin-2-one 在 [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]gold bis(trifluoromethanesulfonyl)imidate 作用下, 以 1,2-二氯乙烷 为溶剂, 生成 2,4,6-trimethyl-N-(1-(2-oxooxazolidin-3-yl)hex-2-enylidene)benzenesulfonamide 、 2,4,6-trimethyl-N-(1-(2-oxooxazolidin-3-yl)hex-2-enylidene)benzenesulfonamide
    参考文献:
    名称:
    Gold-Catalyzed Nitrene Transfer to Activated Alkynes: Formation of α,β-Unsaturated Amidines
    摘要:
    A gold-catalyzed intermolecular nitrene transfer to alkynes was developed for the first time, revealing a new mode of nitrene transfer and providing a novel access to versatile alpha-imino metal carbenes. Various mild nitrene-transfer reagents were examined, and iminopyridium ylides especially those based on 3,5-dichloropyridine proved be highly effective. With activated alkynes such as N-alkynyloxazolidinones as substrates, alpha,beta-unsaturated amidines were formed in mostly good yields.
    DOI:
    10.1021/ol2002607
  • 作为产物:
    描述:
    2,4,6-三甲基苯磺酰氯三乙胺 作用下, 以 四氢呋喃 为溶剂, 以60%的产率得到
    参考文献:
    名称:
    Gold-Catalyzed Nitrene Transfer to Activated Alkynes: Formation of α,β-Unsaturated Amidines
    摘要:
    A gold-catalyzed intermolecular nitrene transfer to alkynes was developed for the first time, revealing a new mode of nitrene transfer and providing a novel access to versatile alpha-imino metal carbenes. Various mild nitrene-transfer reagents were examined, and iminopyridium ylides especially those based on 3,5-dichloropyridine proved be highly effective. With activated alkynes such as N-alkynyloxazolidinones as substrates, alpha,beta-unsaturated amidines were formed in mostly good yields.
    DOI:
    10.1021/ol2002607
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