Frustrated Lewis pairs in two-dimensional borocarbonitride for the facile synthesis of 3-aminoimidazo[1,2-α]pyridines using TMSCN as an isonitrile substitute-Reference-Cited by-同舟云学术

Frustrated Lewis pairs in two-dimensional borocarbonitride for the facile synthesis of 3-aminoimidazo[1,2-α]pyridines using TMSCN as an isonitrile substitute

Published:2024 Issue:13 Volume:48 Page:5971-5980
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Leng Jing¹,Ali Mohd Sajid²,Al-Lohedan Hamad A.²,Rout Chandra Sekhar³,Pramoda K.³,Sharath Kumar Kothanahally S.⁴^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Yangzhou Polytechnic Institute, Yangzhou, Jiangsu 225127, P. R. China

2. Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

3. Centre for Nano and Material Sciences, Jain (Deemed-to-be-University), Jain Global Campus, Kanakapura, Bangalore 562112, India

4. Department of Studies in Chemistry, Manasagangotri, University of Mysore, Mysore 570006, India

Abstract

Reusable catalysts are attractive alternatives to the metal-free catalysts accelerating the Groebke–Blackburn–Bienayme reaction for the efficient synthesis of imidazo[1,2-α]pyridines.

Funder

Natural Science Research of Jiangsu Higher Education Institutions of China

King Saud University

Science and Engineering Research Board

Vision Group on Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D4NJ00302K

Reference43 articles.

1. Synthesis of new set of imidazo[1,2-a]pyridine-schiff bases derivatives as potential antimicrobial agents: Experimental and theoretical approaches

2. Groebke Blackburn Bienaymé-mediated multi-component synthesis of selective HDAC6 inhibitors with anti-inflammatory properties

3. Recent developments of imidazo[1,2-a]pyridine analogues as antituberculosis agents

4. Imidazopyridine-based kinase inhibitors as potential anticancer agents: A review

5. Antiulcer agents. 5. Inhibition of gastric H+/K+-ATPase by substituted imidazo[1,2-a]pyridines and related analogs and its implication in modeling the high affinity potassium ion binding site of the gastric proton pump enzyme

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