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(4R,5R)-2-Ethyl-2-methyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[((R)-2-hydroxy-1-phenyl-ethyl)-amide] | 528840-93-9

中文名称
——
中文别名
——
英文名称
(4R,5R)-2-Ethyl-2-methyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[((R)-2-hydroxy-1-phenyl-ethyl)-amide]
英文别名
——
(4R,5R)-2-Ethyl-2-methyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[((R)-2-hydroxy-1-phenyl-ethyl)-amide]化学式
CAS
528840-93-9
化学式
C24H30N2O6
mdl
——
分子量
442.512
InChiKey
ZGFBQBFJKLVTHW-UWHLTILDSA-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):
    1.6
  • 重原子数:
    32.0
  • 可旋转键数:
    9.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    117.12
  • 氢给体数:
    4.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    (4R,5R)-2-Ethyl-2-methyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[((R)-2-hydroxy-1-phenyl-ethyl)-amide]sodium hydroxide三乙胺 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 反应 2.83h, 生成 all(R)-4,5-bis[4-Ph-oxazolin-2-yl]-2-Me-2-Et-[1,3]-dioxolane
    参考文献:
    名称:
    Enantioselective Mercuriocyclization of γ-Hydroxy-cis-alkenes
    摘要:
    Asymmetric mercuriocyclization of gamma-hydroxy-(Z)-alkenes has been achieved using Hg(II) complexed with tartrate-derived 4-(2-naphthyl)bisoxazoline as chiral ligand to give rise to 2-monosubstituted tetrahydrofurans in 86-95% ee. Not only the linker connecting two oxazolines but also their 4-substituents were found crucial for high enantioselectivity. In addition, tuning the ketal protecting group of tartrate as well as adding MeOH and K(2)CO(3) worked beneficially.
    DOI:
    10.1021/ja029777d
  • 作为产物:
    描述:
    O,O'-sec-butylidene-Lg-tartaric acid dimethyl esterD-苯甘氨醇氰化钠 作用下, 反应 5.0h, 以75%的产率得到(4R,5R)-2-Ethyl-2-methyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[((R)-2-hydroxy-1-phenyl-ethyl)-amide]
    参考文献:
    名称:
    Enantioselective Mercuriocyclization of γ-Hydroxy-cis-alkenes
    摘要:
    Asymmetric mercuriocyclization of gamma-hydroxy-(Z)-alkenes has been achieved using Hg(II) complexed with tartrate-derived 4-(2-naphthyl)bisoxazoline as chiral ligand to give rise to 2-monosubstituted tetrahydrofurans in 86-95% ee. Not only the linker connecting two oxazolines but also their 4-substituents were found crucial for high enantioselectivity. In addition, tuning the ketal protecting group of tartrate as well as adding MeOH and K(2)CO(3) worked beneficially.
    DOI:
    10.1021/ja029777d
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