Issue 54, 2016, Issue in Progress

Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones

Abstract

A KOH-promoted regiospecific synthesis of polysubstituted N-(2-pyridyl)pyrroles under transition metal-free conditions has been developed. The pyrrole and pyridine rings were simultaneously installed from acyclic enaminone precursors under mild conditions and generated 1 equiv. of H2O as the sole byproduct. A series of polysubstituted N-(2-pyridyl)pyrroles were provided in up to 91% yield for 21 examples.

Graphical abstract: Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones

Supplementary files

Article information

Article type
Paper
Submitted
07 Apr 2016
Accepted
12 May 2016
First published
12 May 2016

RSC Adv., 2016,6, 48905-48909

Author version available

Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones

J. Shen, X. Yang, F. Wang, Y. Wang, G. Cheng and X. Cui, RSC Adv., 2016, 6, 48905 DOI: 10.1039/C6RA08987A

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