Skeleton Editing of Benzothiazoles to Spiro[benzothiazole-<i>n</i>-alkanes] by Carbon-to-Carbon Single-Atom Swapping

Skeleton editing can be used to precisely replace or rearrange atoms in the core ring structure of complex molecules and is often used to modify heteroaromatic compounds. However, this approach has not been used to modify thiazole rings. We report the direct construction of spiro[benzothiazole-<i>n</i>-alkanes] through skeleton editing of thiazolium salts by carbon-to-carbon single-atom swapping. Skeleton editing via carbon deletion and insertion has the advantages of high efficiency, high selectivity, simple operation, and one-step, metal-catalyst-free construction of novel spirocyclic products with novel structures.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-03-06
DOI
https://doi.org/10.1021/acs.joc.4c02876
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81

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article

Skeleton Editing of Benzothiazoles to Spiro[benzothiazole-n-alkanes] by Carbon-to-Carbon Single-Atom Swapping

Zhongzhi Zhu, Lanyu Li, Zhen-Lin Hou, Xiuwen Chen et al.
3 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
2.81
article

Skeleton Editing of Benzothiazoles to Spiro[benzothiazole-n-alkanes] by Carbon-to-Carbon Single-Atom Swapping

Zhongzhi Zhu, Lanyu Li, Zhen-Lin Hou, Xiuwen Chen, Muze Lin, Yuqun Lin, Tong Yu, Tianxiang Chen, Guozhang Fu
article en
3 citations

Abstract

Skeleton editing can be used to precisely replace or rearrange atoms in the core ring structure of complex molecules and is often used to modify heteroaromatic compounds. However, this approach has not been used to modify thiazole rings. We report the direct construction of spiro[benzothiazole-<i>n</i>-alkanes] through skeleton editing of thiazolium salts by carbon-to-carbon single-atom swapping. Skeleton editing via carbon deletion and insertion has the advantages of high efficiency, high selectivity, simple operation, and one-step, metal-catalyst-free construction of novel spirocyclic products with novel structures.

The Journal of Organic ChemistryVol. 90(11)
Hong Kong Polytechnic University (HK), Guilin Medical University (CN), Wuyi University (CN)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, Fundo para o Desenvolvimento das Ciências e da Tecnologia, Wuyi University, Department of Education of Guangdong Province
Openalex Percentile: Top 12%
Catalytic C–H Functionalization Methods
2.81
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