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Electronic effect of substituents on anilines favors 1,4-addition to trans-β-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles†‡
Radhakrishna Gattu,Suchandra Bhattacharjee,Karuna Mahato,Abu T. Khan
Organic & Biomolecular Chemistry Pub Date : 04/24/2018 00:00:00 , DOI:10.1039/C8OB00736E
Abstract

A simple and an efficient method for the regioselective synthesis of N-alkyl/aryl/H 3-arylindole derivatives from N-substituted anilines and trans-β-nitrostyrenes has been described using 10 mol% of bismuth(III) triflate as a catalyst in acetonitrile at 80 °C. The present protocol profits from the formation of new C–C and C–N bonds, broad substrate scope and moderate to good yields.

Graphical abstract: Electronic effect of substituents on anilines favors 1,4-addition to trans-β-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles
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