Copper-Catalyzed Radical-Triggered Annulation–Halocyanomethylation Reaction of Alkynyl-Bearing Bicyclo[1.1.0]butanes (BCBs) Leading to Spirocyclobutyl Quinolinones

The novel copper-catalyzed radical-triggered annulation-halocyanomethylation reaction, involving preprepared alkynyl-substituted bicyclo[1.1.0]butanes (BCBs) and haloacetonitrile, was reported for the first time, enabling the synthesis of various halocyanomethylated spirocyclobutyl quinolinones with moderate to high yields and perfect regioselectivity. This method exhibits broad substrate adaptability and exceptional functional group tolerance and is distinguished by its capacity to directly form up to three new chemical bonds while constructing a spirocyclic framework in a single step.

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Publication Details

Journal
Organic Letters
Published
2025-11-14
DOI
https://doi.org/10.1021/acs.orglett.5c04128
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81
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article

Copper-Catalyzed Radical-Triggered Annulation–Halocyanomethylation Reaction of Alkynyl-Bearing Bicyclo[1.1.0]butanes (BCBs) Leading to Spirocyclobutyl Quinolinones

Jianwu Liu, Jia Zeng, Pengcheng Xu, Hang‐Dong Zuo et al.
3 citations
Organic Letters
Catalytic C–H Functionalization Methods
2.81
article

Copper-Catalyzed Radical-Triggered Annulation–Halocyanomethylation Reaction of Alkynyl-Bearing Bicyclo[1.1.0]butanes (BCBs) Leading to Spirocyclobutyl Quinolinones

Jianwu Liu, Jia Zeng, Pengcheng Xu, Hang‐Dong Zuo, Yu‐Ting Wang, Shanshan Zhu, Zou Xiao
article en
3 citations

Abstract

The novel copper-catalyzed radical-triggered annulation-halocyanomethylation reaction, involving preprepared alkynyl-substituted bicyclo[1.1.0]butanes (BCBs) and haloacetonitrile, was reported for the first time, enabling the synthesis of various halocyanomethylated spirocyclobutyl quinolinones with moderate to high yields and perfect regioselectivity. This method exhibits broad substrate adaptability and exceptional functional group tolerance and is distinguished by its capacity to directly form up to three new chemical bonds while constructing a spirocyclic framework in a single step.

Organic LettersVol. 27(47)
The First People’s Hospital of Lianyungang (CN), Hua Medicine (China) (CN), Changzhou University (CN), Huaiyin Institute of Technology (CN), Lianyungang Technical College
Openalex Percentile: Top 9%
Catalytic C–H Functionalization Methods
2.81
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Copper-Catalyzed Radical-Triggered Annulation–Halocyanomethylation Reaction of Alkynyl-Bearing Bicyclo[1.1.0]butanes (BCBs) Leading to Spirocyclobutyl Quinolinones — Jianwu Liu, Jia Zeng, et al. · Organic Letters (2025) | TGRS Research Map | TGRS