Direct Synthesis of 3,4‐Disubstituted Quinolines and 2‐Acylquinolines from Amines and Epoxides

Abstract Herein, we present a protocol starting from styrene oxide reacting with o ‐acylaniline and o ‐alkenylaniline derivatives to obtain 3,4‐disubstituted quinoline and 2‐acylquinoline derivatives, respectively, in 32–92% yields under specific conditions. Preliminary research outcomes underscore the versatility of our approach, as exemplified by its scalability for large‐scale synthesis, downstream derivatization, and the characteristic properties manifested by the modified molecules.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-10-22
DOI
https://doi.org/10.1002/adsc.202401055
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.50
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article

Direct Synthesis of 3,4‐Disubstituted Quinolines and 2‐Acylquinolines from Amines and Epoxides

Bingchuan Yang, Shuai Fang, Shichen Li, Chen Ma et al.
2 citations
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
0.50
article

Direct Synthesis of 3,4‐Disubstituted Quinolines and 2‐Acylquinolines from Amines and Epoxides

Bingchuan Yang, Shuai Fang, Shichen Li, Chen Ma, Xiaotian Wu, Xueyan Lv
article en
2 citations

Abstract

Abstract Herein, we present a protocol starting from styrene oxide reacting with o ‐acylaniline and o ‐alkenylaniline derivatives to obtain 3,4‐disubstituted quinoline and 2‐acylquinoline derivatives, respectively, in 32–92% yields under specific conditions. Preliminary research outcomes underscore the versatility of our approach, as exemplified by its scalability for large‐scale synthesis, downstream derivatization, and the characteristic properties manifested by the modified molecules.

Advanced Synthesis & CatalysisVol. 367(4)
Ministry of Education of the People's Republic of China (CN), Shandong University (CN), Education University of Hong Kong (HK), Qilu Normal University (CN), University of Hong Kong (HK)
Openalex Percentile: Top 38%
Catalytic C–H Functionalization Methods
0.50
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