Enatioselective[2+2+2] Cycloaddition as A Synthetic Tool

被引:0
作者
T.Shibata
S.Yoshida
M.Otsuka
Y.Arai
K.Endo
机构
[1] DepartmentofChemistryandBiochemistry,SchoolofAdvancedScienceandEngineering,WasedaUniversity,Okubo,Shinjuku,Tokyo-,Japan
关键词
axial chirality; catalysis; cycloaddition; transition metal; polyaryl;
D O I
10.15943/j.cnki.fdxb-jns.2007.05.039
中图分类号
O621.25 [];
学科分类号
摘要
<正>1 Results Transition metal-catalyzed [2+2+2] cycloaddition is one of the most efficient protocols for the construction of six-membered ring system.Our group has comprehensively studied various types of highly enantioselective [2+2+2] cycloaddition for the synthesis of chiral cycloadducts; we already reported an iridium-catalyzed intermolecular [2+2+2] cycloaddition between α,ω-diynes,having various tethers and substituents on the alkyne termini,and monoalkynes,possessing oxygen or/and nitrogen functionalities at the propargylic position(s)[1].See scheme 1.
引用
收藏
页码:587 / 587
页数:1
相关论文
共 2 条
  • [1] Shibata T,Arai Y,Takami K,et al. Adv Syn&Cat . 2006
  • [2] Shibata T,Fuji moto T,Yokota K,et al. Journal of the American Chemical Society . 2004