A Concise Method for Constructing Pyrrolo[1,2-a]quinoxaline Derivatives via Pictet–Spengler Type Cyclization

A simple and efficient method for concise synthesis of pyrido[3,2-e]pyrrolo[1,2-a]pyrazine deriva­tives based on Pictet–Spengler type cyclization reaction has been successfully developed. This procedure tolerates different types of aldehydes and ketones as starting materials in the presence of trifluoroacetic acid to provide the desired heterocyclic products with medium to excellent yields. The heterocycle containing bromine could be further used as a building block to synthesize more complex compounds. This strategy is characterized by simple operation and environmental friendliness and is a reliable tool for synthesizing bioactive substances.

Authors

Institutions

Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2024-10-01
DOI
https://doi.org/10.1134/s1070428024100178
Citations
1
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.25
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Concise Method for Constructing Pyrrolo[1,2-a]quinoxaline Derivatives via Pictet–Spengler Type Cyclization

Feng Liu, J. Chen, Xuebin Yu, Xiaojuan Zhu et al.
1 citations
Russian Journal of Organic Chemistry
Synthesis and Biological Evaluation
0.25
article

A Concise Method for Constructing Pyrrolo[1,2-a]quinoxaline Derivatives via Pictet–Spengler Type Cyclization

Feng Liu, J. Chen, Xuebin Yu, Xiaojuan Zhu, Yang Liu, Yuewei Zhang
article en
1 citations

Abstract

A simple and efficient method for concise synthesis of pyrido[3,2-e]pyrrolo[1,2-a]pyrazine deriva­tives based on Pictet–Spengler type cyclization reaction has been successfully developed. This procedure tolerates different types of aldehydes and ketones as starting materials in the presence of trifluoroacetic acid to provide the desired heterocyclic products with medium to excellent yields. The heterocycle containing bromine could be further used as a building block to synthesize more complex compounds. This strategy is characterized by simple operation and environmental friendliness and is a reliable tool for synthesizing bioactive substances.

Russian Journal of Organic ChemistryVol. 60(10)
Beijing Institute of Petrochemical Technology (CN), Jilin University of Chemical Technology (CN), Changchun Bureau of Science and Technology (CN)
Openalex Percentile: Top 45%
Synthesis and Biological Evaluation
0.25
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.