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(1'R/S,2'R,3'S)-3-[3'-(3-furyl)-1'-hydroxy-2'-methyl-cyclopent-2'-yl]-propanol | 448961-16-8

中文名称
——
中文别名
——
英文名称
(1'R/S,2'R,3'S)-3-[3'-(3-furyl)-1'-hydroxy-2'-methyl-cyclopent-2'-yl]-propanol
英文别名
(2R,3S)-3-(furan-3-yl)-2-(3-hydroxypropyl)-2-methylcyclopentan-1-ol
(1'R/S,2'R,3'S)-3-[3'-(3-furyl)-1'-hydroxy-2'-methyl-cyclopent-2'-yl]-propanol化学式
CAS
448961-16-8
化学式
C13H20O3
mdl
——
分子量
224.3
InChiKey
PEZMMUGAHCUAHB-LKOMHFJYSA-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:
    16
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    53.6
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (1'R/S,2'R,3'S)-3-[3'-(3-furyl)-1'-hydroxy-2'-methyl-cyclopent-2'-yl]-propanol草酰氯二甲基亚砜三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 2.58h, 生成 (2E,2'R,3'R)-methyl 2-bromo-5-[3'-(3-furyl)-2'-methyl-1'-oxocyclopent-2'-yl]-pent-2-enoate
    参考文献:
    名称:
    A Convergent Synthesis of the Cardenolide Skeleton:  Intramolecular Aldol Condensation via Reduction of α-Bromoketones
    摘要:
    Synthesis of the highly biologically valuable cardenolide backbone was achieved via anionic polycyclization. Bromoketone 18, obtained from double-Michael cycloaddition between cyclohexenone 14 and gamma,delta-unsaturated beta-ketoester 16, was efficiently aldolized under reductive conditions. The highly functionalized tetracyclic compound 52 is an important synthetic intermediate that is potentially amenable to natural cardenolide total synthesis.
    DOI:
    10.1021/jo025612b
  • 作为产物:
    描述:
    参考文献:
    名称:
    A Convergent Synthesis of the Cardenolide Skeleton:  Intramolecular Aldol Condensation via Reduction of α-Bromoketones
    摘要:
    Synthesis of the highly biologically valuable cardenolide backbone was achieved via anionic polycyclization. Bromoketone 18, obtained from double-Michael cycloaddition between cyclohexenone 14 and gamma,delta-unsaturated beta-ketoester 16, was efficiently aldolized under reductive conditions. The highly functionalized tetracyclic compound 52 is an important synthetic intermediate that is potentially amenable to natural cardenolide total synthesis.
    DOI:
    10.1021/jo025612b
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