Issue 5, 2018

A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5′-nucleotidase inhibitory effects

Abstract

A new and efficient domino reaction of 3-chlorochromones with electron-rich aminoheterocycles was developed which allows for a convenient synthesis of a variety of pyrazolo[3,4-b]pyridines, pyrrolo[2,3-b]pyridines, pyrido[2,3-d]pyrimidines and benzofuro[3,2-b]pyridines. The products exhibit strong fluorescence. In addition, they exhibit significant ecto-5′-nucleotidase inhibition properties and cytotoxic behavior.

Graphical abstract: A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5′-nucleotidase inhibitory effects

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2017
Accepted
22 Dec 2017
First published
22 Dec 2017

Org. Biomol. Chem., 2018,16, 717-732

A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5′-nucleotidase inhibitory effects

M. Miliutina, J. Janke, S. Hassan, S. Zaib, J. Iqbal, J. Lecka, J. Sévigny, A. Villinger, A. Friedrich, S. Lochbrunner and P. Langer, Org. Biomol. Chem., 2018, 16, 717 DOI: 10.1039/C7OB02729J

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