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(Z)-5-benzyldimethylsilyl-2-isopropyl-4-pentenoic acid | 639086-27-4

中文名称
——
中文别名
——
英文名称
(Z)-5-benzyldimethylsilyl-2-isopropyl-4-pentenoic acid
英文别名
——
(Z)-5-benzyldimethylsilyl-2-isopropyl-4-pentenoic acid化学式
CAS
639086-27-4
化学式
C17H26O2Si
mdl
——
分子量
290.478
InChiKey
JZSPFDUVGPEOOY-WQLSENKSSA-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

反应信息

  • 作为反应物:
    描述:
    (Z)-5-benzyldimethylsilyl-2-isopropyl-4-pentenoic acid对甲苯磺酸 作用下, 以 氯仿 为溶剂, 反应 12.0h, 生成 trans-2-benzyldimethylsilylmethyl-4-isopropyltetrahydrofuran
    参考文献:
    名称:
    Acid-catalyzed intramolecular addition of a carboxy group to vinylsilanes
    摘要:
    In the presence of a catalytic amount of (TsOHH2O)-H-. or TiCl4, 5-silyl-4-pentenoic acids (1), namely vinylsilanes with a carboxy group, were smoothly cyclized to gamma-lactones in good to high yields. The difference in the geometry of the carbon-carbon double-bond did not affect the reaction rate. The TiCl4-catalyzed cyclization of the substrates bearing a phenyl or alkyl group at the homoallylic position showed moderate cis-selectivity, while introduction of a substituent into the allylic position led to high transselectivity. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(03)00533-3
  • 作为产物:
    描述:
    (Z)-5-(Benzyl-dimethyl-silanyl)-2-isopropyl-pent-4-en-1-ol 在 重铬酸吡啶 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 20.0h, 生成 (Z)-5-benzyldimethylsilyl-2-isopropyl-4-pentenoic acid
    参考文献:
    名称:
    Acid-catalyzed intramolecular addition of a carboxy group to vinylsilanes
    摘要:
    In the presence of a catalytic amount of (TsOHH2O)-H-. or TiCl4, 5-silyl-4-pentenoic acids (1), namely vinylsilanes with a carboxy group, were smoothly cyclized to gamma-lactones in good to high yields. The difference in the geometry of the carbon-carbon double-bond did not affect the reaction rate. The TiCl4-catalyzed cyclization of the substrates bearing a phenyl or alkyl group at the homoallylic position showed moderate cis-selectivity, while introduction of a substituent into the allylic position led to high transselectivity. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(03)00533-3
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