Different catalytic approaches of Friedländer synthesis of quinolines

Bibliographic Details
Title: Different catalytic approaches of Friedländer synthesis of quinolines
Authors: Indhu Chandrasekaran, S. Sarveswari
Source: Heliyon, Vol 11, Iss 2, Pp e41709- (2025)
Publisher Information: Elsevier, 2025.
Publication Year: 2025
Collection: LCC:Science (General)
LCC:Social sciences (General)
Subject Terms: Friedländer synthesis, Polysubstituted quinolines, Ionic liquids, Nanocatalysts, Metal-organic frameworks, Organocatalysts, Science (General), Q1-390, Social sciences (General), H1-99
More Details: Friedländer quinoline synthesis is one of the most important and simplest methods among the various reported methodologies for quinoline synthesis, renowned for its efficiency and versatility. The reaction involves the condensation of a 2-aminobenzaldehyde with a ketone, forming polysubstituted quinolines. This review comprehensively examined diverse catalytic approaches developed to optimize the Friedländer reaction, highlighting recent advancements and their impact on reaction efficiency, selectivity, and environmental sustainability. The discussion encompassed traditional catalysts and emerging catalytic systems, including ionic liquids, metal-organic frameworks, polymers, and nanocatalysts. Additionally, the review addresses the influence of various catalytic environments on reaction outcomes. By collating and critically analyzing recent advancements, this review aims to provide a valuable resource for researchers seeking to leverage these catalytic strategies for synthesizing quinoline derivatives.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2405-8440
Relation: http://www.sciencedirect.com/science/article/pii/S2405844025000891; https://doaj.org/toc/2405-8440
DOI: 10.1016/j.heliyon.2025.e41709
Access URL: https://doaj.org/article/6b499391dc17431ba239ee974bdea00d
Accession Number: edsdoj.6b499391dc17431ba239ee974bdea00d
Database: Directory of Open Access Journals
More Details
ISSN:24058440
DOI:10.1016/j.heliyon.2025.e41709
Published in:Heliyon
Language:English