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N-[2-[8-[[hydroxy-[8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carbonyl]oxycarbonyl-4-(2-methylpropoxy)quinolin-8-yl]-8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carboximidic acid | 1260822-81-8

中文名称
——
中文别名
——
英文名称
N-[2-[8-[[hydroxy-[8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carbonyl]oxycarbonyl-4-(2-methylpropoxy)quinolin-8-yl]-8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carboximidic acid
英文别名
——
N-[2-[8-[[hydroxy-[8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carbonyl]oxycarbonyl-4-(2-methylpropoxy)quinolin-8-yl]-8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carboximidic acid化学式
CAS
1260822-81-8
化学式
C104H110N12O19
mdl
——
分子量
1832.09
InChiKey
ILDVFAAOSDUGDV-KNTAELDDSA-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):
    22.6
  • 重原子数:
    135
  • 可旋转键数:
    34
  • 环数:
    16.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    424
  • 氢给体数:
    6
  • 氢受体数:
    31

反应信息

  • 作为产物:
    描述:
    三乙胺 作用下, 以 氯仿 为溶剂, 反应 24.2h, 以0.087 g的产率得到N-[2-[8-[[hydroxy-[8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carbonyl]oxycarbonyl-4-(2-methylpropoxy)quinolin-8-yl]-8-[[hydroxy-[8-[[hydroxy-[(1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptan-1-yl]methylidene]amino]-4-(2-methylpropoxy)quinolin-2-yl]methylidene]amino]-4-(2-methylpropoxy)quinoline-2-carboximidic acid
    参考文献:
    名称:
    喹啉低聚酰胺中螺旋惯性的绝对控制
    摘要:
    据报道,喹啉衍生的螺旋折叠的芳族寡酰胺在其N端被各种手性官能团官能化。当引入(1 S)-(-)-樟脑基部分时,发现在质子传递和非质子传递溶剂中,螺旋旋性都完全转变为右旋螺旋度(de> 99%)。绝对螺旋感和de值通过1 H NMR,圆二色性(CD)和X射线晶体学进行了明确表征。这些化合物的晶体结构使我们能够基于空间因素和分子内氢键的结合,为诱导螺旋旋向性的效率提出理论依据。
    DOI:
    10.1021/jo1019442
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