Bi(OTf)3-Catalyzed Diastereoselective Three-Component Povarov Reaction of Aminoquinones toward Tetrahydroquinolinequinones

We have developed a Bi(OTf)3-catalyzed three-component Povarov reaction of aminoquinones, aldehydes, and olefins that provides straightforward, one-step access to highly substituted 1,2,3,4-tetrahydroquinolinequinones in isolated yields of up to 96%, with diastereoselectivities ranging from 1.6:1 to >20:1. Mechanistic studies using E- and Z-alkene probes support a stepwise cationic pathway rather than a concerted cycloaddition, which rationalizes the observed stereochemical outcomes. The synthetic utility is further highlighted by subsequent oxidative dehydrogenation to afford quinolinequinone derivatives, a class of molecules of significant biological relevance.

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-10-28
DOI
https://doi.org/10.1021/acs.joc.6c01919
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Bi(OTf)3-Catalyzed Diastereoselective Three-Component Povarov Reaction of Aminoquinones toward Tetrahydroquinolinequinones

Shaozhong Wang, Guixuan Zhao
1 links
The Journal of Organic Chemistry
Multicomponent Synthesis of Heterocycles
article

Bi(OTf)3-Catalyzed Diastereoselective Three-Component Povarov Reaction of Aminoquinones toward Tetrahydroquinolinequinones

Shaozhong Wang, Guixuan Zhao
article en

Abstract

We have developed a Bi(OTf)3-catalyzed three-component Povarov reaction of aminoquinones, aldehydes, and olefins that provides straightforward, one-step access to highly substituted 1,2,3,4-tetrahydroquinolinequinones in isolated yields of up to 96%, with diastereoselectivities ranging from 1.6:1 to >20:1. Mechanistic studies using E- and Z-alkene probes support a stepwise cationic pathway rather than a concerted cycloaddition, which rationalizes the observed stereochemical outcomes. The synthetic utility is further highlighted by subsequent oxidative dehydrogenation to afford quinolinequinone derivatives, a class of molecules of significant biological relevance.

The Journal of Organic Chemistry
Nanjing University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 26%
Multicomponent Synthesis 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.

Laika access coming soon