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(1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20 acetate | 1103491-75-3

中文名称
——
中文别名
——
英文名称
(1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20 acetate
英文别名
[(1S,4S,6S,9Z,12S,15S)-15-hydroxy-4,15,16,16-tetramethyl-5-oxatricyclo[10.3.1.04,6]hexadec-9-en-9-yl]methyl acetate
(1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20 acetate化学式
CAS
1103491-75-3
化学式
C22H36O4
mdl
——
分子量
364.525
InChiKey
GXUUJFVYGVUSPX-MTGCWZIMSA-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):
    3.4
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    59.1
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20 acetatesodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 2.0h, 以64%的产率得到(1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol
    参考文献:
    名称:
    Oxygenated verticillene derivatives from Bursera suntui
    摘要:
    Medium polarity fractions of the hexane extracts of the stems of Bursera suntui afforded six previously known (1-6) and four hitherto unknown verticillane derivatives: (1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol (7), (1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20-acetate (8), (1S,3Z,7S,11S,12S)-(+)-verticilla-3,8(19)-dien-7,12,20-triol (9), and (1S,3Z,7S,11S,12S)-(+)-verticilla-3, 8(19)-dien-7,12,20-triol 20-acetate (10). Acetylation of 9 and 10 yielded (IS,3Z7S,1IS,12S)-(+)-verticilla-3,8(19)-dien-7,12,20-triol 7.20-diacetate (11), while hydrolysis of 8 gave 7. The structures and stereochemistry of 7-11 were established by spectroscopic analyses, particularly by 1D and 2D NMR spectra and HRESIMS. The conformational preferences of 7-11 were studied by molecular mechanics modelling employing the Monte Carlo protocol followed by B3LYP/DGDZVP DFT calculation, thus supporting the observed H-1 NMR NOESY cross peaks. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2008.09.013
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