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dimethyl 5-(4,4-dimethyl-2-oxooxazolidin-3-yl)-6-(2-hydroxy-6-methylphenyl)-4,7-dimethyl-1,3-dihydro-2H-indene-2,2-dicarboxylate | 1174417-44-7

中文名称
——
中文别名
——
英文名称
dimethyl 5-(4,4-dimethyl-2-oxooxazolidin-3-yl)-6-(2-hydroxy-6-methylphenyl)-4,7-dimethyl-1,3-dihydro-2H-indene-2,2-dicarboxylate
英文别名
——
dimethyl 5-(4,4-dimethyl-2-oxooxazolidin-3-yl)-6-(2-hydroxy-6-methylphenyl)-4,7-dimethyl-1,3-dihydro-2H-indene-2,2-dicarboxylate化学式
CAS
1174417-44-7
化学式
C27H31NO7
mdl
——
分子量
481.546
InChiKey
MGACMCOWHNAMJN-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):
    4.15
  • 重原子数:
    35.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    102.37
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    A rhodium(I)-xylyl-BINAP catalyzed asymmetric ynamide-[2+2+2] cycloaddition in the synthesis of optically enriched N,O-biaryls
    摘要:
    A rhodium(I)-xylyl-BINAP catalyzed asymmetric [2+2+2] cycloaddition of achiral conjugated aryl ynamides with various diynes is described here. This asymmetric cycloaddition provides a series of structurally interesting chiral N,O-biaryls with excellent enantioselectivity along with a modest diastereoselectivity, with respect to both C-C and C-N axial chirality. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.03.078
  • 作为产物:
    描述:
    Dimethyl 5-(4,4-dimethyl-2-oxo-1,3-oxazolidin-3-yl)-6-(2-methoxy-6-methylphenyl)-4,7-dimethyl-1,3-dihydroindene-2,2-dicarboxylate 在 三溴化硼 作用下, 以 二氯甲烷 为溶剂, 以67%的产率得到dimethyl 5-(4,4-dimethyl-2-oxooxazolidin-3-yl)-6-(2-hydroxy-6-methylphenyl)-4,7-dimethyl-1,3-dihydro-2H-indene-2,2-dicarboxylate
    参考文献:
    名称:
    A rhodium(I)-xylyl-BINAP catalyzed asymmetric ynamide-[2+2+2] cycloaddition in the synthesis of optically enriched N,O-biaryls
    摘要:
    A rhodium(I)-xylyl-BINAP catalyzed asymmetric [2+2+2] cycloaddition of achiral conjugated aryl ynamides with various diynes is described here. This asymmetric cycloaddition provides a series of structurally interesting chiral N,O-biaryls with excellent enantioselectivity along with a modest diastereoselectivity, with respect to both C-C and C-N axial chirality. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.03.078
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