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(2R,4R)-2,4-dimethyl-5-oxotetrahydrofuran-2-carboxylic acid | 950489-52-8

中文名称
——
中文别名
——
英文名称
(2R,4R)-2,4-dimethyl-5-oxotetrahydrofuran-2-carboxylic acid
英文别名
(2R,4R)-2,4-dimethyl-5-oxooxolane-2-carboxylic acid
(2R,4R)-2,4-dimethyl-5-oxotetrahydrofuran-2-carboxylic acid化学式
CAS
950489-52-8
化学式
C7H10O4
mdl
——
分子量
158.154
InChiKey
NWZNGXRJSXHFFN-CLZZGJSISA-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):
    0.41
  • 重原子数:
    11.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    63.6
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Preparation of enantiopure 3,5,5-trialkyl-γ-butyrolactones by diastereospecific 5-endo halo lactonizations
    摘要:
    A new preparation of 3,5,5-trialkyl-gamma-butyrolactones of defined absolute configuration is reported. This method involves the diastereoselective alkylation of 3,4-ethylenic acids after incorporation of a chiral Evans auxiliary, and then after separation of the two diastereomers and hydrolysis of the auxiliary, stereospecific halo lactonizations. This method was applied to the preparation of a natural product, present in a sponge. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2007.05.028
  • 作为产物:
    参考文献:
    名称:
    Preparation of enantiopure 3,5,5-trialkyl-γ-butyrolactones by diastereospecific 5-endo halo lactonizations
    摘要:
    A new preparation of 3,5,5-trialkyl-gamma-butyrolactones of defined absolute configuration is reported. This method involves the diastereoselective alkylation of 3,4-ethylenic acids after incorporation of a chiral Evans auxiliary, and then after separation of the two diastereomers and hydrolysis of the auxiliary, stereospecific halo lactonizations. This method was applied to the preparation of a natural product, present in a sponge. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2007.05.028
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