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Ethyl (4S)-4-hydroxy-7-iodo-6-methylhept-6-en-2-ynoate | 918313-66-3

中文名称
——
中文别名
——
英文名称
Ethyl (4S)-4-hydroxy-7-iodo-6-methylhept-6-en-2-ynoate
英文别名
ethyl (4S)-4-hydroxy-7-iodo-6-methylhept-6-en-2-ynoate
Ethyl (4S)-4-hydroxy-7-iodo-6-methylhept-6-en-2-ynoate化学式
CAS
918313-66-3
化学式
C10H13IO3
mdl
——
分子量
308.116
InChiKey
DVUANUMLMTVKSL-SECBINFHSA-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

物化性质

  • 沸点:
    353.0±42.0 °C(Predicted)
  • 密度:
    1.617±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:731bbcb5bd62a33aac119919d1ff5936
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反应信息

  • 作为反应物:
    描述:
    Ethyl (4S)-4-hydroxy-7-iodo-6-methylhept-6-en-2-ynoate 在 sodium tetrahydroborate 、 copper(l) chloride 作用下, 以 甲醇 为溶剂, 反应 0.25h, 生成
    参考文献:
    名称:
    A strategy toward the synthesis of C13-oxidized cembrenolides
    摘要:
    An efficient strategy for the construction of C-13-oxidized cembrenolides is reported. Central to this strategy is the installation of the C-13 hydroxyl group prior to cembrane macrocyclization (via formation of the C-1-C-2 bond), allowing access to both C-13 alcohol epimers. The orientation of the C-13 alcohol was found to influence the cyclization mode of the cembranolide scaffold upon furan oxidation, leading to motifs reminiscent to bipinnatolide F, bielschowskysin, and verrillin. (c) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.01.085
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文献信息

  • A strategy toward the synthesis of C13-oxidized cembrenolides
    作者:Alec Saitman、Steven D.E. Sullivan、Emmanuel A. Theodorakis
    DOI:10.1016/j.tetlet.2013.01.085
    日期:2013.3
    An efficient strategy for the construction of C-13-oxidized cembrenolides is reported. Central to this strategy is the installation of the C-13 hydroxyl group prior to cembrane macrocyclization (via formation of the C-1-C-2 bond), allowing access to both C-13 alcohol epimers. The orientation of the C-13 alcohol was found to influence the cyclization mode of the cembranolide scaffold upon furan oxidation, leading to motifs reminiscent to bipinnatolide F, bielschowskysin, and verrillin. (c) 2013 Elsevier Ltd. All rights reserved.
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