Issue 4, 2022

Simple inorganic base promoted polycyclic construction using mucohalic acid as a C3 synthon: synthesis and AIE probe application of benzo[4,5]imidazo[1,2-a]pyridines

Abstract

A transition metal-free and efficient synthesis of fused azapolycycles via a multicomponent reaction has been developed using mucohalic acid as a C3 synthon. The reaction promoted by the simple inorganic base K2CO3 gives serial C1-functionalized benzo[4,5]imidazo[1,2-a]pyridine products using symmetrical and unsymmetrical substrates with satisfactory yields. What is more, the target compound 4a as a representative example exhibits the aggregation-induced emission (AIE) property, and its AIE performance can be applied to effectively sense picric acid (PA) with a detection limit and quenching constant of 1.15 × 10–7 M and 3.39 × 104 M−1, respectively.

Graphical abstract: Simple inorganic base promoted polycyclic construction using mucohalic acid as a C3 synthon: synthesis and AIE probe application of benzo[4,5]imidazo[1,2-a]pyridines

Supplementary files

Article information

Article type
Research Article
Submitted
24 Nov 2021
Accepted
13 Jan 2022
First published
13 Jan 2022

Org. Chem. Front., 2022,9, 1127-1136

Simple inorganic base promoted polycyclic construction using mucohalic acid as a C3 synthon: synthesis and AIE probe application of benzo[4,5]imidazo[1,2-a]pyridines

K. Yang, Z. Chen, Y. Zhou, Q. Chen, S. Yu, S. Luo and Z. Wang, Org. Chem. Front., 2022, 9, 1127 DOI: 10.1039/D1QO01753E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements