论文成果
Highly beta(Z)-Selective Hydrosilylation of Terminal Alkynes Catalyzed by Thiolate-Bridged Dirhodium Complexes
  • 点击次数:
  • 论文类型:期刊论文
  • 发表时间:2018-09-07
  • 发表刊物:ORGANIC LETTERS
  • 收录刊物:SCIE
  • 文献类型:J
  • 卷号:20
  • 期号:17
  • 页面范围:5357-5361
  • ISSN号:1523-7060
  • 摘要:A series of novel monothiolate-bridged dirhodium complexes, [Cp*Rh(mu-SR)(mu-Cl)(2)RhCp*][BF4] {Cp* = eta(5)-C5Me5, R = tertiary butyl (Bu-t), 1a; R = ferrocenyl (Fc), 1b; R = adamantyl (Ad), 1c} were designed and successfully synthesized, which can smoothly facilitate highly regioselective and stereoselective hydrosilylation of terminal alkynes to afford beta(Z) vinylsilanes with good functional group compatibility. Furthermore, the hydride bridged dirhodium complex [Cp*Rh(mu-(SBu)-Bu-t)(mu-Cl)(mu-H)RhCp*][BF4] (5) as a potential inter-mediate was obtained by the reaction of la with excess HSiEt3.

上一条: Iodine-mediated cross-dehydrogenative coupling of pyrazolones and alkenes

下一条: Synthesis of 2-trifluoromethyl-2-hydroxy-2H-chromenes via cyclization of (Z)-trifluoromethyl alkenyl triflates and salicylaldehydes