摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(1'S,2R,3S)-2-(2'-methylenecyclopentyl)-5-oxotetrahydrofuran-3-carbaldehyde | 913969-12-7

中文名称
——
中文别名
——
英文名称
(1'S,2R,3S)-2-(2'-methylenecyclopentyl)-5-oxotetrahydrofuran-3-carbaldehyde
英文别名
(2R,3S)-2-[(1S)-2-methylidenecyclopentyl]-5-oxooxolane-3-carbaldehyde
(1'S,2R,3S)-2-(2'-methylenecyclopentyl)-5-oxotetrahydrofuran-3-carbaldehyde化学式
CAS
913969-12-7
化学式
C11H14O3
mdl
——
分子量
194.23
InChiKey
JKUGUVKNYJIXCS-YWVKMMECSA-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):
    1.47
  • 重原子数:
    14.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    (1'S,2R,3S)-2-(2'-methylenecyclopentyl)-5-oxotetrahydrofuran-3-carbaldehyde三氟化硼乙醚三甲胺 作用下, 以 二氯甲烷 为溶剂, 生成 (1'RS,1''S,4R,5R)-4-(1'-trimethylsilanyloxybut-3'-enyl)-5-(2''-methylenecyclopentyl)-4,5-dihydrofuran-2(3H)-one
    参考文献:
    名称:
    Facile Asymmetric Synthesis of the Core Nuclei of Xanthanolides, Guaianolides, and Eudesmanolides
    摘要:
    Bicylic and tricyclic gamma-butyrolactones with 5,7-, 5,6,5-, 5,6,6-, or 5,7,5-fused ring systems, being found in xanthanolides, eudesmanolides, and guaianolides, were readily synthesized from methyl furan-2-carboxylic acid. Key steps were a copper(I)-catalyzed asymmetric cyclopropanation, Sakurai allylations, intramolecular ene reactions, and ring-closing metathesis reactions.
    DOI:
    10.1021/ol034141s
  • 作为产物:
    描述:
    参考文献:
    名称:
    Facile Asymmetric Synthesis of the Core Nuclei of Xanthanolides, Guaianolides, and Eudesmanolides
    摘要:
    Bicylic and tricyclic gamma-butyrolactones with 5,7-, 5,6,5-, 5,6,6-, or 5,7,5-fused ring systems, being found in xanthanolides, eudesmanolides, and guaianolides, were readily synthesized from methyl furan-2-carboxylic acid. Key steps were a copper(I)-catalyzed asymmetric cyclopropanation, Sakurai allylations, intramolecular ene reactions, and ring-closing metathesis reactions.
    DOI:
    10.1021/ol034141s
点击查看最新优质反应信息