Zn/H<sub>2</sub>O-mediated tandem reductive cyclization of 2-(2-nitrophenyl)-1<i>H</i>-benzo[<i>d</i>]imidazoles with aldehydes to synthesize 5,6-dihydrobenzo[4,5]imidazo[1,2-<i>c</i>]quinazolines

A one-pot tandem approach to synthesize 5,6-dihydrobenzo[4,5]imidazo[1,2-<i>c</i>]quinolones has been developed from 2-(2-nitrophenyl)-1<i>H</i>-benzo[<i>d</i>]imidazoles and aldehydes <i>via</i> a Zn/H<sub>2</sub>O-mediated reductive cyclization process, characterised by cheap and readily available raw materials, a simple, green, economical and efficient protocol, good product yields and product diversity.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d4ob01976h
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
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article

Zn/H2O-mediated tandem reductive cyclization of 2-(2-nitrophenyl)-1H-benzo[d]imidazoles with aldehydes to synthesize 5,6-dihydrobenzo[4,5]imidazo[1,2-c]quinazolines

Guisheng Zhang, Zhenhua Guo, Xiaopeng Zhang, Zihua Yang et al.
Organic & Biomolecular Chemistry
Quinazolinone synthesis and applications
article

Zn/H2O-mediated tandem reductive cyclization of 2-(2-nitrophenyl)-1H-benzo[d]imidazoles with aldehydes to synthesize 5,6-dihydrobenzo[4,5]imidazo[1,2-c]quinazolines

Guisheng Zhang, Zhenhua Guo, Xiaopeng Zhang, Zihua Yang, Qiuyang Pang
article en

Abstract

A one-pot tandem approach to synthesize 5,6-dihydrobenzo[4,5]imidazo[1,2-<i>c</i>]quinolones has been developed from 2-(2-nitrophenyl)-1<i>H</i>-benzo[<i>d</i>]imidazoles and aldehydes <i>via</i> a Zn/H<sub>2</sub>O-mediated reductive cyclization process, characterised by cheap and readily available raw materials, a simple, green, economical and efficient protocol, good product yields and product diversity.

Organic & Biomolecular ChemistryVol. 23(15)
Henan Normal University (CN)
Openalex Percentile: Top 96%
Quinazolinone synthesis and applications
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