Palladium‐Catalyzed Dihalogenative Cyclization of Amide‐Fused 1,6‐Enynes for the Synthesis of Lactams

Owing to their unique properties, the synthesis of α ‐methylenelactams has long been a research hotspot in synthetic chemistry. In this article, a Pd‐catalyzed intramolecular dihalogenative cyclization reaction of amide‐fused 1,6‐enynes was developed, which successfully afforded a series of α ‐methylenelactam compounds. This reaction exhibits advantages including good yields, excellent stereoselectivity, and favorable functional group tolerance. In addition, the synthetic application of the products showed that the halogens reserved in the products can further undergo reactions such as cross‐coupling reactions and substitution reactions.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-01-07
DOI
https://doi.org/10.1002/ejoc.202501151
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
22.95

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article

Palladium‐Catalyzed Dihalogenative Cyclization of Amide‐Fused 1,6‐Enynes for the Synthesis of Lactams

Luning Tang, Xiang Li, Hai Huang, Shan Zhong
1 citations
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
22.95
article

Palladium‐Catalyzed Dihalogenative Cyclization of Amide‐Fused 1,6‐Enynes for the Synthesis of Lactams

Luning Tang, Xiang Li, Hai Huang, Shan Zhong
article en
1 citations

Abstract

Owing to their unique properties, the synthesis of α ‐methylenelactams has long been a research hotspot in synthetic chemistry. In this article, a Pd‐catalyzed intramolecular dihalogenative cyclization reaction of amide‐fused 1,6‐enynes was developed, which successfully afforded a series of α ‐methylenelactam compounds. This reaction exhibits advantages including good yields, excellent stereoselectivity, and favorable functional group tolerance. In addition, the synthetic application of the products showed that the halogens reserved in the products can further undergo reactions such as cross‐coupling reactions and substitution reactions.

European Journal of Organic ChemistryVol. 29(6)
Changzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 3%
Catalytic C–H Functionalization Methods
22.95
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