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1,3-bis(4-fluorophenyl)prop-2-ynyl methyl carbonate | 1191257-26-7

中文名称
——
中文别名
——
英文名称
1,3-bis(4-fluorophenyl)prop-2-ynyl methyl carbonate
英文别名
——
1,3-bis(4-fluorophenyl)prop-2-ynyl methyl carbonate化学式
CAS
1191257-26-7
化学式
C17H12F2O3
mdl
——
分子量
302.277
InChiKey
RZLIZWFYCZUEBL-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):
    4.3
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1,3-bis(4-fluorophenyl)prop-2-ynyl methyl carbonatebenzyl (2-hydroxyphenyl)acetatetris(dibenzylideneacetone)dipalladium(0) chloroform complex 、 1,1'-bis(diphenylphosphino)ferrocene 作用下, 以 二甲基亚砜 为溶剂, 以66%的产率得到(3SR,4RS,Z)-benzyl 2-(4-fluorobenzylidene)-3-(4-fluorophenyl)chroman-4-carboxylate
    参考文献:
    名称:
    Stereoselective Construction of Substituted Chromans by Palladium-Catalyzed Cyclization of Propargylic Carbonates with 2-(2-Hydroxyphenyl)acetates
    摘要:
    Highly substituted chromans have been constructed in a highly stereoselective manner by a palladium-catalyzed reaction of propargylic carbonates with 2-(2-hydroxyphenyl)acetates. Enantioselective reactions also successfully proceeded to give the optically active chromans with high enantioselectivity.
    DOI:
    10.1021/ol901964z
  • 作为产物:
    描述:
    1,3-bis(4-fluorophenyl)prop-2-yn-1-ol 、 氯甲酸甲酯吡啶 作用下, 以 二氯甲烷 为溶剂, 以96%的产率得到1,3-bis(4-fluorophenyl)prop-2-ynyl methyl carbonate
    参考文献:
    名称:
    Stereoselective Construction of Substituted Chromans by Palladium-Catalyzed Cyclization of Propargylic Carbonates with 2-(2-Hydroxyphenyl)acetates
    摘要:
    Highly substituted chromans have been constructed in a highly stereoselective manner by a palladium-catalyzed reaction of propargylic carbonates with 2-(2-hydroxyphenyl)acetates. Enantioselective reactions also successfully proceeded to give the optically active chromans with high enantioselectivity.
    DOI:
    10.1021/ol901964z
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文献信息

  • Synthesis of Substituted Tetrahydrocyclobuta[<i>b</i>]benzofurans by Palladium-Catalyzed Substitution/[2+2] Cycloaddition of Propargylic Carbonates with 2-Vinylphenols
    作者:Masahiro Yoshida、Shoko Ohno、Kosuke Namba
    DOI:10.1002/anie.201306903
    日期:2013.12.16
    Radical methods: The title reaction proceeds in the presence of a palladium catalyst to deliver substituted tetrahydrocyclobuta[b]benzofurans in a stereoselective manner (see scheme). A radical mechanism is discussed.
    自由基方法:标题反应在钯催化剂的存在下进行,以立体选择性方式递送取代的四氢环丁[ b ]苯并呋喃(参见方案)。讨论了一种根本机制。
  • Stereoselective Construction of Substituted Chromans by Palladium-Catalyzed Cyclization of Propargylic Carbonates with 2-(2-Hydroxyphenyl)acetates
    作者:Masahiro Yoshida、Mariko Higuchi、Kozo Shishido
    DOI:10.1021/ol901964z
    日期:2009.10.15
    Highly substituted chromans have been constructed in a highly stereoselective manner by a palladium-catalyzed reaction of propargylic carbonates with 2-(2-hydroxyphenyl)acetates. Enantioselective reactions also successfully proceeded to give the optically active chromans with high enantioselectivity.
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