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Benzylidene succinimides as 3C synthons for the asymmetric tandem Mannich reaction/transamidation of cyclic trifluoromethyl ketimines to obtain F3C-containing polycyclic dihydroquinazolinones.

Xia-Yan ZhangPei-Hao DouWen-Ya LuYong YouJian-Qiang ZhaoZhen-Hua WangWei-Cheng Yuan
Published in: Chemical communications (Cambridge, England) (2021)
By taking advantage of benzylidene succinimides as a new class of 3C synthons, a highly diastereo- and enantioselective tandem Mannich reaction/transamidation has been established by reacting them with cyclic trifluoromethyl N-acyl ketimines. Using a Cinchona alkaloid-derived squaramide as the catalyst, the tandem reaction proceeded smoothly under mild conditions and afforded a range of F3C-containing chiral polycyclic dihydroquinazolinones with excellent results (up to 99% yield, all cases >20 : 1 dr, up to 99% ee).
Keyphrases
  • ionic liquid
  • electron transfer
  • room temperature
  • highly efficient
  • metal organic framework