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Chiral phosphoric acid catalyzed enantioselective N-alkylation of indoles with in situ generated cyclic N-acyl ketimines†
Lvye Zhang,Binqiang Wu,Zhangtao Chen,Jinjin Hu,Xiaofei Zeng,Guofu Zhong
Chemical Communications Pub Date : 07/26/2018 00:00:00 , DOI:10.1039/C8CC05073B
Abstract

A chiral SPINOL derived phosphoric acid-catalyzed asymmetric N-alkylation reaction of indoles with cyclic α-diaryl-substituted N-acyl imines, which are generated in situ from 3-aryl 3-hydroxyisoindolinones, has been demonstrated. The transformation proceeds smoothly with a broad range of indoles and isoindolinone alcohols. A variety of indole derived N-alkylated tetrasubstituted chiral aminals were afforded in moderate to good yields (50–79%) with excellent enantioselectivities (up to 98% ee).

Graphical abstract: Chiral phosphoric acid catalyzed enantioselective N-alkylation of indoles with in situ generated cyclic N-acyl ketimines
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