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1-[4-[3-(4-Nitrophenyl)sulfonyl-2-phenyl-1,3-oxazolidin-4-yl]phenyl]ethanone | 1253298-01-9

中文名称
——
中文别名
——
英文名称
1-[4-[3-(4-Nitrophenyl)sulfonyl-2-phenyl-1,3-oxazolidin-4-yl]phenyl]ethanone
英文别名
——
1-[4-[3-(4-Nitrophenyl)sulfonyl-2-phenyl-1,3-oxazolidin-4-yl]phenyl]ethanone化学式
CAS
1253298-01-9
化学式
C23H20N2O6S
mdl
——
分子量
452.488
InChiKey
DTWWMOHGYHOUPD-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):
    3.4
  • 重原子数:
    32
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    118
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    1-(4-乙烯基-苯基)-乙酮2-((4-nitrophenyl)sulfonyl)-3-phenyl-1,2-oxaziridine四丁基氯化铵 、 copper dichloride 作用下, 以 二氯甲烷 为溶剂, 反应 1.5h, 以59%的产率得到1-[4-[3-(4-Nitrophenyl)sulfonyl-2-phenyl-1,3-oxazolidin-4-yl]phenyl]ethanone
    参考文献:
    名称:
    N-Nosyl oxaziridines as terminal oxidants in copper(II)-catalyzed olefin oxyaminations
    摘要:
    We report that N-4-nosyl-3-phenyloxaziridine is an effective terminal oxidant for copper(II)-catalyzed oxyamination recently developed in our labs. This oxaziridine can be prepared on multi-gram scale and is easily purified by recrystallization. The products of oxyamination using this oxaziridine bear protecting groups that can be readily removed in high yields under mild conditions. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.08.015
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文献信息

  • N-Nosyl oxaziridines as terminal oxidants in copper(II)-catalyzed olefin oxyaminations
    作者:Sandra M. DePorter、Ashley C. Jacobsen、Katherine M. Partridge、Kevin S. Williamson、Tehshik P. Yoon
    DOI:10.1016/j.tetlet.2010.08.015
    日期:2010.10
    We report that N-4-nosyl-3-phenyloxaziridine is an effective terminal oxidant for copper(II)-catalyzed oxyamination recently developed in our labs. This oxaziridine can be prepared on multi-gram scale and is easily purified by recrystallization. The products of oxyamination using this oxaziridine bear protecting groups that can be readily removed in high yields under mild conditions. (C) 2010 Elsevier Ltd. All rights reserved.
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