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- W2080494121 endingPage "852" @default.
- W2080494121 startingPage "847" @default.
- W2080494121 abstract "An organocatalytic quadruple domino reaction initiated by a Friedel–Crafts-type reaction of electron-rich arenes is described. The procedure involving up to three different Michael acceptors afforded highly functionalized cyclohexenecarbaldehydes bearing an aniline moiety, which are of great pharmaceutical and agricultural interest. This diphenylprolinol trimethylsilyl ether-catalyzed reaction also generates up to 4 contiguous stereocenters. It could be shown that various functional groups are tolerated and all products were obtained with very good diastereo- and excellent enantioselectivity." @default.
- W2080494121 created "2016-06-24" @default.
- W2080494121 creator A5064146592 @default.
- W2080494121 creator A5075542756 @default.
- W2080494121 creator A5080205433 @default.
- W2080494121 creator A5088754757 @default.
- W2080494121 date "2013-02-28" @default.
- W2080494121 modified "2023-10-16" @default.
- W2080494121 title "An Asymmetric Organocatalytic Quadruple Cascade Initiated by a Friedel-Crafts-Type Reaction with Electron-Rich Arenes" @default.
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