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cis-2-methyl-3-(ethoxycarbonyl)-1,8-dioxabicyclo<4.3.0>non-2-ene | 82469-40-7

中文名称
——
中文别名
——
英文名称
cis-2-methyl-3-(ethoxycarbonyl)-1,8-dioxabicyclo<4.3.0>non-2-ene
英文别名
cis-(3a,7a)-3-Ethoxycarbonyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo[2,3-b]pyran;cis(3a,7a)-3-ethoxycarbonyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo<2,3-b>pyran;ethyl 2-methyl-4,5,6,7a-tetrahydro-3aH-furo[2,3-b]pyran-3-carboxylate;ethyl (3aS,7aR)-2-methyl-4,5,6,7a-tetrahydro-3aH-furo[2,3-b]pyran-3-carboxylate
cis-2-methyl-3-(ethoxycarbonyl)-1,8-dioxabicyclo<4.3.0>non-2-ene化学式
CAS
82469-40-7
化学式
C11H16O4
mdl
——
分子量
212.246
InChiKey
KNTABPYFNXDNFY-GZMMTYOYSA-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):
    1.4
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3,4-二氢-2H-吡喃重氮基乙酰乙酸乙酯六氟乙酰丙酮化铜的水合物 作用下, 以 氯苯 为溶剂, 以67%的产率得到cis-2-methyl-3-(ethoxycarbonyl)-1,8-dioxabicyclo<4.3.0>non-2-ene
    参考文献:
    名称:
    Studies on the origin of dihydrofurans from .alpha.-diazocarbonyl compounds. Concerted 1,3-dipolar cycloaddition vs. nonsynchronous coupling in the copper chelate catalyzed reactions of .alpha.-diazodicarbonyl compounds with electron-rich olefins
    摘要:
    DOI:
    10.1021/jo00140a030
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文献信息

  • Synthesis of fused acetal derivatives by manganic acetate promoted additions to endocyclic enol ethers
    作者:John M. Mellor、Shahid Mohammed
    DOI:10.1016/s0040-4020(01)87230-6
    日期:1993.8
    Reaction of manganic acetate in acetic acid with β-diketones and β-ketoesters leads to generation of intermediates, which add efficiently to endocyclic unsaturated enol ethers to afford fused acetals.
    乙酸乙酸中与β-二酮和β-酮​​酸酯的反应导致生成中间体,该中间体可有效地添加到环内不饱和烯醇醚中以提供稠合缩醛
  • Tetrabutylammonium Peroxydisulfate in Organic Synthesis; IX: A Convenient Approach to the Synthesis of Fused Acetal Derivatives by Tetrabutylammonium Peroxydisulfate-Mediated Oxidative Cycloaddition of 1,3-Dicarbonyl Compounds to Cyclic Enol Ethers
    作者:Fen-Er Chen、Han Fu、Ge Meng、Yu Cheng、Ye-Li Hu
    DOI:10.1055/s-2000-6312
    日期:——
    A number of fused acetal derivatives were prepared in 82-90% yield by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-diketones or 1,3-diketoesters to cyclic enol ethers in the presence of a base such as potassium acetate in acetonitrile.
    通过四丁基过氧化二硫酸介导的 1,3-二酮或 1,3-二酮酯与环状烯醇醚在乙腈中的氧化环化反应,制备出了一些融合缩醛生物,收率为 82-90%。
  • Synthesis of fused acetals by ceric ammonium nitrate mediated cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers
    作者:Subhas Chandra Roy、Pijus Kumar Mandal
    DOI:10.1016/0040-4020(96)00728-4
    日期:1996.9
    Treatment of β-diketones and β-ketoesters with ceric ammonium nitrate and sodium hydrogen carbonate in acetonitrile leads to the formation of intermediates which add efficiently to cyclic enol ethers to furnish fused acetals in good yields.
    硝酸铈铵碳酸氢钠乙腈中处理β-二酮和β-酮​​酸酯会导致形成中间体,该中间体可有效地添加到环状烯醇醚中,从而以高收率提供熔融缩醛
  • Efficient One-Pot Synthesis of Multi-Substituted Dihydrofurans by Ruthenium(II)-Catalyzed [3+2] Cycloaddition of Cyclic or Acyclic Diazodicarbonyl Compounds with Olefins
    作者:Likai Xia、Yong Rok Lee
    DOI:10.1002/adsc.201300245
    日期:2013.8.12
    AbstractRuthenium(II)‐phosphine complexes‐catalyzed [3+2] cycloadditions were conducted to synthesize a variety of dihydrofurans by reactions of cyclic or acyclic diazodicarbonyl compounds with olefins. This method represents a direct and efficient one‐pot synthesis for multi‐substituted dihydrofurans under mild reaction conditions with an excellent regioselectivity. Furthermore, to reduce reaction times and increase yields of dihydrofurans, microwave‐assisted tris(triphenylphosphine)ruthenium(II) chloride/ 1‐butyl‐3‐methylimidazolium tetrafluoroborate Ru(PPh3)3Cl2/[Bmim]BF4}‐catalyzed reactions were also developed. The synthesized dihydrofurans can be readily converted into biologically interesting tetrahydroindoles.magnified image
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