Reaction of imidazo[1,2-<i>a</i>]pyridines with coumarin-3-carboxylic acids: a domino Michael addition/decarboxylation/oxidation/annulation-Reference-Cited by-同舟云学术

Reaction of imidazo[1,2-a]pyridines with coumarin-3-carboxylic acids: a domino Michael addition/decarboxylation/oxidation/annulation

Published:2022 Issue:40 Volume:46 Page:19455-19459
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kianmehr Ebrahim¹^ORCID,Bari Bahareh¹,Jafarzadeh Mahdi¹^ORCID,Rostami Ali²^ORCID,Golshani Mostafa³,Foroumadi Alireza³

Affiliation:

1. School of Chemistry, College of Science, University of Tehran, Tehran 1417614411, Iran

2. Natural and Medical Sciences Research Center (NMSRC), University of Nizwa, Nizwa 616, Sultanate of Oman

3. Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

Abstract

A palladium-catalyzed decarboxylative domino reaction of imidazo[1,2-a]pyridines and coumarin-3-carboxylic acids has been developed, which provides access to dibenzoisochromenoimidazo[1,2-a]pyridin-6-ones possessing six fused rings.

Funder

University of Tehran

Iran National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ02706B

Reference40 articles.

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5. Discovery and SAR of Novel and Selective Inhibitors of Urokinase Plasminogen Activator (uPA) with an Imidazo[1,2-a]pyridine Scaffold

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