Catalytic enantioselective synthesis of quaternary 3,3′-indolyloxindoles by combination of Rh(ii) complexes and chiral phosphines†
Abstract
Rh(II)/chiral phosphine combined catalysis has been developed for a highly efficient sequential C–H functionalization/asymmetric allylation or Michael addition reaction of indoles and 3-diazooxindoles with allenoates or vinyl ketones to afford a diverse range of quaternary 3,3′-indolyloxindole derivatives. Moreover, a significantly positive effect of LiCl in the sequential C–H functionalization/allylation reaction was observed, which led to an unusual ternary activation mechanism in the allylation step.
- This article is part of the themed collection: HOT articles in Organic Chemistry Frontiers in 2015