4.8 Article

Cinchona Alkaloid Squaramide/AgOAc Cooperatively Catalyzed Diastereo- and Enantioselective Mannich/Cyclization Cascade Reaction of Isocyanoacetates and Cyclic Trifluoromethyl Ketimines

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ORGANIC LETTERS
卷 16, 期 17, 页码 4566-4569

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AMER CHEMICAL SOC
DOI: 10.1021/ol502123z

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  1. National Natural Science Foundation of China [20772030, 21072056, 21272067]
  2. Fundamental Research Funds for the Central Universities

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An efficient diastereo- and enantioselective Mannich-type/cyclization cascade reaction of alpha-substituted isocyanoacetates and cyclic trifluoromethyl ketimines cooperatively catalyzed by cinchona alkaloid-derived multi-hydrogen-bonding donor squaramide and AgOAc has been investigated, affording the optically active trifluoromethyl-substituted tetrahydroimidazo[1,5-c]-quinazoline derivatives in excellent yields (up to 99%) and good to excellent stereoselectivities (up to >15:1 dr, up to 9896 cc) under mild conditions.

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