Recent Progress in the Synthesis of Indolizine Derivatives

Abstract: Indolizines are N-bridgehead bicyclic heterocyclic compounds with a π-excessive pyrrole and a π-deficient pyridine. These heterocycles widely appear both in nature and in synthetic sources. This subclass of heterocycles possesses a diverse range of bioactivities, such as antimicrobial, anti-inflammatory, anticancer, antiviral, and enzyme inhibitory activities, and several synthetic compounds with an indolizine skeleton have been used as drugs for the treatment of various diseases. In addition, many indolizine derivatives have been employed as important building blocks for the synthesis of many bioactive and heterocyclic compounds. Applications of indolizines in organic materials have also been well documented. Due to the importance of indolizine-based compounds, the development of efficient methods for the synthesis of indolizine derivatives has attracted the attention of chemists, and a number of studies on the synthesis of indolizines have been reported over the years. In this review article, we will give a comprehensive overview of the synthesis of indolizines dating back to 2014. More than 145 studies on the synthesis of indolizine derivatives have been collected and summarized. References have been retrieved from various resources such as Google Scholar, SciFinder, and PubMed. The work might be useful for chemists who work in the synthesis of heterocycles and in medicinal chemistry.

Authors

Institutions

Publication Details

Journal
Current Organic Synthesis
Published
2026-04-01
DOI
https://doi.org/10.2174/0115701794456310260307165955
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Recent Progress in the Synthesis of Indolizine Derivatives

Dau Xuan Duc, Nguyễn Văn Quốc, Nguyễn Thị Chung
Current Organic Synthesis
Synthesis and Reactivity of Heterocycles
article

Recent Progress in the Synthesis of Indolizine Derivatives

Dau Xuan Duc, Nguyễn Văn Quốc, Nguyễn Thị Chung
article en

Abstract

Abstract: Indolizines are N-bridgehead bicyclic heterocyclic compounds with a π-excessive pyrrole and a π-deficient pyridine. These heterocycles widely appear both in nature and in synthetic sources. This subclass of heterocycles possesses a diverse range of bioactivities, such as antimicrobial, anti-inflammatory, anticancer, antiviral, and enzyme inhibitory activities, and several synthetic compounds with an indolizine skeleton have been used as drugs for the treatment of various diseases. In addition, many indolizine derivatives have been employed as important building blocks for the synthesis of many bioactive and heterocyclic compounds. Applications of indolizines in organic materials have also been well documented. Due to the importance of indolizine-based compounds, the development of efficient methods for the synthesis of indolizine derivatives has attracted the attention of chemists, and a number of studies on the synthesis of indolizines have been reported over the years. In this review article, we will give a comprehensive overview of the synthesis of indolizines dating back to 2014. More than 145 studies on the synthesis of indolizine derivatives have been collected and summarized. References have been retrieved from various resources such as Google Scholar, SciFinder, and PubMed. The work might be useful for chemists who work in the synthesis of heterocycles and in medicinal chemistry.

Current Organic SynthesisVol. 23
Vinh University (VN)
Openalex Percentile: Top 21%
Synthesis and Reactivity of Heterocycles
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.