Sustainable synthesis of quinolines and pyrroles enabled by chromium-catalyzed acceptorless dehydrogenative coupling using a bipyridine ligand

A straightforward and atom-economical method for the synthesis of quinolines and pyrroles has been reported. Using Earth-abundant, commercially available CrCl<sub>2</sub> salt as a catalyst and the inexpensive, bench-stable 6,6'-dimethyl-2,2'-dipyridyl as a ligand, this chromium-catalyzed acceptorless dehydrogenative coupling provides important heterocycles, quinolines and pyrroles, in synthetically useful yields with good functional group tolerance, releasing water and hydrogen gas as by-products. Notably, the described protocol was also found to be applicable to the sustainable synthesis of highly substituted fused polycyclic quinolines and pyrroles. Moreover, the synthetic value of this operationally simple protocol was demonstrated by gram-scale synthesis of quinolines.

Authors

Institutions

Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00150a
Citations
3
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Sustainable synthesis of quinolines and pyrroles enabled by chromium-catalyzed acceptorless dehydrogenative coupling using a bipyridine ligand

Zhao Du, Chuanqi Liu, Chen Qing, Xiaoqian Wang et al.
3 citations
Organic & Biomolecular Chemistry
Asymmetric Hydrogenation and Catalysis
1.61
article

Sustainable synthesis of quinolines and pyrroles enabled by chromium-catalyzed acceptorless dehydrogenative coupling using a bipyridine ligand

Zhao Du, Chuanqi Liu, Chen Qing, Xiaoqian Wang, Yilei Wang, Zhihua Peng, Wantong Yue
article en
3 citations

Abstract

A straightforward and atom-economical method for the synthesis of quinolines and pyrroles has been reported. Using Earth-abundant, commercially available CrCl<sub>2</sub> salt as a catalyst and the inexpensive, bench-stable 6,6'-dimethyl-2,2'-dipyridyl as a ligand, this chromium-catalyzed acceptorless dehydrogenative coupling provides important heterocycles, quinolines and pyrroles, in synthetically useful yields with good functional group tolerance, releasing water and hydrogen gas as by-products. Notably, the described protocol was also found to be applicable to the sustainable synthesis of highly substituted fused polycyclic quinolines and pyrroles. Moreover, the synthetic value of this operationally simple protocol was demonstrated by gram-scale synthesis of quinolines.

Organic & Biomolecular ChemistryVol. 23(18)
China University of Petroleum, East China (CN)
Responsible consumption and production
Openalex Percentile: Top 18%
Asymmetric Hydrogenation and Catalysis
1.61
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.

Sustainable synthesis of quinolines and pyrroles enabled by chromium-catalyzed acceptorless dehydrogenative coupling using a bipyridine ligand — Zhao Du, Chuanqi Liu, et al. · Organic & Biomolecular Chemistry (2025) | TGRS Research Map | TGRS