N-Heterocyclic Carbene (NHC) Catalyzed Annulations of δ-Acetoxy Allenoates and Enaminones: A Time-Controlled Regiodivergent Synthesis of Hexahydroquinolines

An NHC (N-heterocyclic carbene) catalyzed [3 + 3] annulation of δ-acetoxy allenoates and enaminones has been developed. This strategy provides a facile and convenient approach for the synthesis of 1,4-dihydropyridine and 3,4-dihydropyridine-based hexahydroquinoline derivatives (51 examples, up to 77% yield). This protocol features a broad substrate scope, good functional group tolerance, and mild reaction conditions. Interestingly, the regioselectivity of products is time-controlled. At the beginning of the reaction, 1,4-dihydropyridines are rapidly formed, and 3,4-dihydropyridines are obtained with the extension of the reaction time.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-01
DOI
https://doi.org/10.1021/acs.joc.5c00685
Citations
2
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
1.87

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article

N-Heterocyclic Carbene (NHC) Catalyzed Annulations of δ-Acetoxy Allenoates and Enaminones: A Time-Controlled Regiodivergent Synthesis of Hexahydroquinolines

Tuanjie Li, Changsheng Yao, Kai Zhang, Yu Zhang et al.
2 citations
The Journal of Organic Chemistry
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
1.87
article

N-Heterocyclic Carbene (NHC) Catalyzed Annulations of δ-Acetoxy Allenoates and Enaminones: A Time-Controlled Regiodivergent Synthesis of Hexahydroquinolines

Tuanjie Li, Changsheng Yao, Kai Zhang, Yu Zhang, Chenxia Yu, Shi Bai
article en
2 citations

Abstract

An NHC (N-heterocyclic carbene) catalyzed [3 + 3] annulation of δ-acetoxy allenoates and enaminones has been developed. This strategy provides a facile and convenient approach for the synthesis of 1,4-dihydropyridine and 3,4-dihydropyridine-based hexahydroquinoline derivatives (51 examples, up to 77% yield). This protocol features a broad substrate scope, good functional group tolerance, and mild reaction conditions. Interestingly, the regioselectivity of products is time-controlled. At the beginning of the reaction, 1,4-dihydropyridines are rapidly formed, and 3,4-dihydropyridines are obtained with the extension of the reaction time.

The Journal of Organic ChemistryVol. 90(36)
Jiangsu Normal University (CN), State Key Laboratory of Synthetic Chemistry (CN), Green Chemistry (PL)
National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province, Natural Science Research of Jiangsu Higher Education Institutions of China
Openalex Percentile: Top 14%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
1.87
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