Issue 42, 2016, Issue in Progress

Convenient synthesis of functionalized pyrrolo[3,4-b]pyridines and pyrrolo[3,4-b]quinolines via three-component reactions

Abstract

A simple protocol for convenient construction of pyrrolo[3,4-b]pyridine skeleton was successfully developed by base promoted three-component reaction of β-enamino imide, aromatic aldehydes and malononitrile as well as its ester and amide derivatives. The similar three-component reaction of β-enamino imide, aromatic aldehydes and cyclic diketones such as dimedone and cyclohexane-1,3-dione afforded functionalized pyrrolo[3,4-b]quinolines in good yields.

Graphical abstract: Convenient synthesis of functionalized pyrrolo[3,4-b]pyridines and pyrrolo[3,4-b]quinolines via three-component reactions

Supplementary files

Article information

Article type
Paper
Submitted
03 Feb 2016
Accepted
02 Apr 2016
First published
05 Apr 2016

RSC Adv., 2016,6, 35609-35616

Convenient synthesis of functionalized pyrrolo[3,4-b]pyridines and pyrrolo[3,4-b]quinolines via three-component reactions

Y. Jiang, M. Xiao and C. Yan, RSC Adv., 2016, 6, 35609 DOI: 10.1039/C6RA03165J

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