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(Z)-2-(benzylthio)-3-phenylacrylic acid | 63546-55-4

中文名称
——
中文别名
——
英文名称
(Z)-2-(benzylthio)-3-phenylacrylic acid
英文别名
(Z)-2-benzylsulfanyl-3-phenylprop-2-enoic acid
(Z)-2-(benzylthio)-3-phenylacrylic acid化学式
CAS
63546-55-4
化学式
C16H14O2S
mdl
——
分子量
270.352
InChiKey
HQOYCRPJAZWDGC-PTNGSMBKSA-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):
    4.1
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    62.6
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    甲醇(Z)-2-(benzylthio)-3-phenylacrylic acid 在 palladium on activated charcoal 氢气 作用下, 生成 methyl 2-(benzylthio)-3-phenylpropanoate
    参考文献:
    名称:
    Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers
    摘要:
    This paper describes the enantio selective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that alpha-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2007.11.020
  • 作为产物:
    描述:
    ethyl 2-(benzylthio)-3-phenylacrylate 在 sodium hydroxide 作用下, 以74%的产率得到(Z)-2-(benzylthio)-3-phenylacrylic acid
    参考文献:
    名称:
    Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers
    摘要:
    This paper describes the enantio selective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that alpha-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2007.11.020
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文献信息

  • Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers
    作者:Alex F. Meindertsma、Michael M. Pollard、Ben L. Feringa、Johannes G. de Vries、Adriaan J. Minnaard
    DOI:10.1016/j.tetasy.2007.11.020
    日期:2007.12
    This paper describes the enantio selective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that alpha-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. (c) 2007 Elsevier Ltd. All rights reserved.
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