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(+)-variabilin

中文名称
——
中文别名
——
英文名称
(+)-variabilin
英文别名
(6aS,11aS)-3,9-dimethoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-6a-ol
(+)-variabilin化学式
CAS
——
化学式
C17H16O5
mdl
——
分子量
300.311
InChiKey
VVPGAJNPGZZNBM-DLBZAZTESA-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):
    1.9
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    57.2
  • 氢给体数:
    1
  • 氢受体数:
    5

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:
    (+)-variabilin二苯基膦酸锂 作用下, 以 二丁醚 为溶剂, 以29%的产率得到3,6,9-三羟基紫檀素
    参考文献:
    名称:
    Asymmetric Total Syntheses of (−)-Variabilin and (−)-Glycinol
    摘要:
    Total syntheses of (-)-variabilin and (-)-glycinol have been accomplished, using the catalytic, asymmetric "Interrupted" Feist-Benary reaction (IFB) as the key transformation to introduce both stereogenic centers. A monoquinidine pyrimidinyl ether catalyst affords the IFB products In over 90% ee in both cases. Other key steps include an intramolecular Buohwald-Hartwig coupling and a nickel-catalyzed aryl tosylate reduction.
    DOI:
    10.1021/ol201332u
  • 作为产物:
    描述:
    6a,11a-dihydro-6a-hydroxy-3,9-dimethoxy-6H-benzofuro[3,2-c]chromen-7-yl 4-methylbenzenesulfonate 在 锂硼氢 、 nickel dichloride 作用下, 以 四氢呋喃 为溶剂, 反应 7.0h, 以90%的产率得到(+)-variabilin
    参考文献:
    名称:
    Asymmetric Total Syntheses of (−)-Variabilin and (−)-Glycinol
    摘要:
    Total syntheses of (-)-variabilin and (-)-glycinol have been accomplished, using the catalytic, asymmetric "Interrupted" Feist-Benary reaction (IFB) as the key transformation to introduce both stereogenic centers. A monoquinidine pyrimidinyl ether catalyst affords the IFB products In over 90% ee in both cases. Other key steps include an intramolecular Buohwald-Hartwig coupling and a nickel-catalyzed aryl tosylate reduction.
    DOI:
    10.1021/ol201332u
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文献信息

  • Synthesis of isoflavonoids. Enantiopure cis- and trans-6a-hydroxypterocarpans and a racemic trans-pterocarpan
    作者:Theunis G van Aardt、Hendrik van Rensburg、Daneel Ferreira
    DOI:10.1016/s0040-4020(01)00679-2
    日期:2001.8
    Aldol condensation between phenylacetates and benzaldehydes affords 2,3-diaryl-3-hydroxypropanoates which serve as common precursors to both the first racemic trans-pterocarpan and enantiopure cis- and trans-6a-hydroxypterocarpans.
    苯乙酸酯和苯甲醛之间的醛醇缩合得到2,3-二芳基-3-羟基丙酸酯,它们是第一个外消旋的反式-罗汉松和对映纯的顺式和反式-6a-羟基罗汉松的常见前体。
  • Asymmetric Total Syntheses of (−)-Variabilin and (−)-Glycinol
    作者:Michael A. Calter、Na Li
    DOI:10.1021/ol201332u
    日期:2011.7.15
    Total syntheses of (-)-variabilin and (-)-glycinol have been accomplished, using the catalytic, asymmetric "Interrupted" Feist-Benary reaction (IFB) as the key transformation to introduce both stereogenic centers. A monoquinidine pyrimidinyl ether catalyst affords the IFB products In over 90% ee in both cases. Other key steps include an intramolecular Buohwald-Hartwig coupling and a nickel-catalyzed aryl tosylate reduction.
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