Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology , Shanghai 200237, P.R. China.
Org Lett. 2014 Sep 5;16(17):4566-9. doi: 10.1021/ol502123z. Epub 2014 Aug 21.
An efficient diastereo- and enantioselective Mannich-type/cyclization cascade reaction of α-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 98% ee) under mild conditions.
一种高效的非对映选择性和对映选择性的 Mannich 型/环化级联反应,由金鸡纳生物碱衍生的多氢键供体双噁唑啉和 AgOAc 共同催化α-取代异氰基乙酸酯和环状三氟甲基亚胺,可以得到光学活性的三氟甲基取代的四氢咪唑并[1,5-c]喹唑啉衍生物,产率优异(高达 99%),立体选择性好至优秀(高达 >15:1 dr,高达 98%ee),条件温和。