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[(2S)-6,7-dichloro-1-methyl-4-oxo-3-oxabicyclo[3.2.0]heptan-2-yl]methyl 2,2-dimethylpropanoate | 697287-54-0

中文名称
——
中文别名
——
英文名称
[(2S)-6,7-dichloro-1-methyl-4-oxo-3-oxabicyclo[3.2.0]heptan-2-yl]methyl 2,2-dimethylpropanoate
英文别名
——
[(2S)-6,7-dichloro-1-methyl-4-oxo-3-oxabicyclo[3.2.0]heptan-2-yl]methyl 2,2-dimethylpropanoate化学式
CAS
697287-54-0
化学式
C13H18Cl2O4
mdl
——
分子量
309.19
InChiKey
XDHOHXMJUGQHQG-RMORJWIASA-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

物化性质

  • 沸点:
    417.2±45.0 °C(Predicted)
  • 密度:
    1.29±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    [(2S)-6,7-dichloro-1-methyl-4-oxo-3-oxabicyclo[3.2.0]heptan-2-yl]methyl 2,2-dimethylpropanoate 作用下, 以 四氢呋喃乙醚乙醇 为溶剂, 反应 3.33h, 生成 (1S)-1-[(1S,4R)-4-(1-hydroxy-1-methylethyl)-1-methyl-2-cyclobutenyl]ethane-1,2-diol
    参考文献:
    名称:
    Highly Efficient and Diastereoselective Synthesis of (+)-Lineatin
    摘要:
    A linear sequence was used to synthesize (+)-lineatin in 14 steps and 14% overall yield from a homochiral 2(5H)-furanone. Key steps of this synthetic approach feature the diastereoselective construction of a cyclobutene through a photochemical [2 + 2] cycloaddition and a regiocontrolled oxymercuration reaction.
    DOI:
    10.1021/ol0497032
  • 作为产物:
    描述:
    顺-1,2-二氯乙烯(-)-(S)-4-methyl-5-pivaloyloxymethyl-2(5H)-furanone乙腈 为溶剂, 反应 7.5h, 以89%的产率得到[(2S)-6,7-dichloro-1-methyl-4-oxo-3-oxabicyclo[3.2.0]heptan-2-yl]methyl 2,2-dimethylpropanoate
    参考文献:
    名称:
    Highly Efficient and Diastereoselective Synthesis of (+)-Lineatin
    摘要:
    A linear sequence was used to synthesize (+)-lineatin in 14 steps and 14% overall yield from a homochiral 2(5H)-furanone. Key steps of this synthetic approach feature the diastereoselective construction of a cyclobutene through a photochemical [2 + 2] cycloaddition and a regiocontrolled oxymercuration reaction.
    DOI:
    10.1021/ol0497032
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文献信息

  • Photocycloaddition of (Z)-1,2-dichloroethylene to enantiopure 2(5H)-furanones: an efficient strategy for the diastereoselective synthesis of cyclobutane and cyclobutene derivatives
    作者:Ramon Alibés、Pedro de March、Marta Figueredo、Josep Font、Marta Racamonde、Albert Rustullet、Angel Alvarez-Larena、Juan F. Piniella、Teodor Parella
    DOI:10.1016/s0040-4039(02)02528-5
    日期:2003.1
    A highly stereoselective and efficient synthetic approach to cyclobutane and cyclobutene derivatives has been developed consisting of a [2+2] photochemical cycloaddition of chiral 2(5H)-furanones to (Z)-1,2-dichloroethylene followed by dihydrodehalogenation or dihaloelimination.
    已经开发了对环丁烷和环丁烯衍生物的高度立体选择性和有效的合成方法,该方法包括将手性2(5 H)-呋喃酮与(Z)-1,2-二氯乙烯进行[2 + 2]光化学环加成,然后进行二氢脱卤或二卤代消除。
  • Highly Efficient and Diastereoselective Synthesis of (+)-Lineatin
    作者:Ramon Alibés、Pedro de March、Marta Figueredo、Josep Font、Marta Racamonde、Teodor Parella
    DOI:10.1021/ol0497032
    日期:2004.4.1
    A linear sequence was used to synthesize (+)-lineatin in 14 steps and 14% overall yield from a homochiral 2(5H)-furanone. Key steps of this synthetic approach feature the diastereoselective construction of a cyclobutene through a photochemical [2 + 2] cycloaddition and a regiocontrolled oxymercuration reaction.
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