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1-[2-(4-Methoxyphenyl)sulfanylphenyl]hexan-2-one | 1190852-59-5

中文名称
——
中文别名
——
英文名称
1-[2-(4-Methoxyphenyl)sulfanylphenyl]hexan-2-one
英文别名
1-[2-(4-methoxyphenyl)sulfanylphenyl]hexan-2-one
1-[2-(4-Methoxyphenyl)sulfanylphenyl]hexan-2-one化学式
CAS
1190852-59-5
化学式
C19H22O2S
mdl
——
分子量
314.448
InChiKey
VPVKVRPNQGYUON-UHFFFAOYSA-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):
    5
  • 重原子数:
    22
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Gold(I)-Catalyzed Intermolecular Oxyarylation of Alkynes: Unexpected Regiochemistry in the Alkylation of Arenes
    摘要:
    The reaction between acetylenes and sulfoxides, studied as a test case for gold-catalyzed intermolecular addition, provides the oxyarylation compounds 3 in good yields. Unpredictably, in all cases a single regioisomer arising from the electrophilic aromatic alkylation at the position adjacent to the sulfur atom is obtained instead of the expected Friedel-Crafts regioisomer. A new concerted mechanism based on DFT calculations is proposed to account for the products in this intermolecular gold(I)-catalyzed reaction.
    DOI:
    10.1021/ol9020578
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文献信息

  • Gold(I)-Catalyzed Intermolecular Oxyarylation of Alkynes: Unexpected Regiochemistry in the Alkylation of Arenes
    作者:Ana B. Cuenca、Sergi Montserrat、Kabir M. Hossain、Gisela Mancha、Agustí Lledós、Mercedes Medio-Simón、Gregori Ujaque、Gregorio Asensio
    DOI:10.1021/ol9020578
    日期:2009.11.5
    The reaction between acetylenes and sulfoxides, studied as a test case for gold-catalyzed intermolecular addition, provides the oxyarylation compounds 3 in good yields. Unpredictably, in all cases a single regioisomer arising from the electrophilic aromatic alkylation at the position adjacent to the sulfur atom is obtained instead of the expected Friedel-Crafts regioisomer. A new concerted mechanism based on DFT calculations is proposed to account for the products in this intermolecular gold(I)-catalyzed reaction.
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