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(8R)-(1-hydroxy-2-methylpropan-2-y)-5-methylcyclonon-(4E)-enone | 1013330-36-3

中文名称
——
中文别名
——
英文名称
(8R)-(1-hydroxy-2-methylpropan-2-y)-5-methylcyclonon-(4E)-enone
英文别名
(4E,8R)-8-(1-hydroxy-2-methylpropan-2-yl)-5-methylcyclonon-4-en-1-one
(8R)-(1-hydroxy-2-methylpropan-2-y)-5-methylcyclonon-(4E)-enone化学式
CAS
1013330-36-3
化学式
C14H24O2
mdl
——
分子量
224.343
InChiKey
PGWNQLFVWFDFND-JXDHDYMSSA-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):
    2.3
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (8R)-(1-hydroxy-2-methylpropan-2-y)-5-methylcyclonon-(4E)-enone对甲苯磺酰氯吡啶 作用下, 反应 12.0h, 以71%的产率得到2-methyl-(2R)-[4-methyl-8-oxocyclonon-(4E)-enyl]propyl 4-methylbenzenesulfonate
    参考文献:
    名称:
    An Unconventional Approach to the Enantioselective Synthesis of Caryophylloids
    摘要:
    The chiral enones 4 and ent-4 have been synthesized enantiomerically as configurationally stable compounds that can be used for the synthesis of caryophylloids. For instance, ent-4 has been converted to the marine natural product coraxeniolide A.
    DOI:
    10.1021/ja8003705
  • 作为产物:
    描述:
    1-甲氧基-1-(三甲基甲硅氧基)-2-甲基-1-丙烯 、 (2Z,6E)-6-methylcyclonona-2,6-dien-1-one 在 triphenylmethyl perchlorate 二异丁基氢化铝triethylamine tris(hydrogen fluoride) 作用下, 以 二氯甲烷正己烷四氢呋喃 为溶剂, 反应 2.67h, 以84%的产率得到(8R)-(1-hydroxy-2-methylpropan-2-y)-5-methylcyclonon-(4E)-enone
    参考文献:
    名称:
    An Unconventional Approach to the Enantioselective Synthesis of Caryophylloids
    摘要:
    The chiral enones 4 and ent-4 have been synthesized enantiomerically as configurationally stable compounds that can be used for the synthesis of caryophylloids. For instance, ent-4 has been converted to the marine natural product coraxeniolide A.
    DOI:
    10.1021/ja8003705
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文献信息

  • An Unconventional Approach to the Enantioselective Synthesis of Caryophylloids
    作者:Oleg V. Larionov、E. J. Corey
    DOI:10.1021/ja8003705
    日期:2008.3.1
    The chiral enones 4 and ent-4 have been synthesized enantiomerically as configurationally stable compounds that can be used for the synthesis of caryophylloids. For instance, ent-4 has been converted to the marine natural product coraxeniolide A.
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