Pd-Catalyzed Dual C–H Activation/Cyclization: Convergent and Divergent Synthesis of 1-Azahelicenes

Herein, we report a convergent synthesis of 1-azahelicenes using easily available quinoline derivatives and cyclic diaryliodonium salts as starting materials. This reaction undergoes a palladium-catalyzed dual C-H activation/cyclization process to give facile access to a wide range of 1-aza[5]helicenes and 1-aza[6]helicenes with abundant functional groups (including F, Cl, Br, I, CF<sub>3</sub>, SeR, SR, and heteroaryl) in moderate to excellent yields, thereby providing new opportunities to fine-tune the properties of the helicene backbone. In addition, the obtained products could be further transformed into helicene-based Lewis base catalysts and redox switch materials easily. Notably, one selected 1-azahelicene shined bright yellow light by aggregation. These features enlarge the chemical space of 1-azahelicenes and inspire further utilization in other areas of research.

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Publication Details

Journal
Organic Letters
Published
2024-10-16
DOI
https://doi.org/10.1021/acs.orglett.4c03136
Citations
5
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.25

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article

Pd-Catalyzed Dual C–H Activation/Cyclization: Convergent and Divergent Synthesis of 1-Azahelicenes

Huikang Fang, Zhong‐Jian Cai, Yixin Xu, Hongkun Li et al.
5 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.25
article

Pd-Catalyzed Dual C–H Activation/Cyclization: Convergent and Divergent Synthesis of 1-Azahelicenes

Huikang Fang, Zhong‐Jian Cai, Yixin Xu, Hongkun Li, Yuqing Liang, Shun‐Jun Ji, Wenru Liu
article en
5 citations

Abstract

Herein, we report a convergent synthesis of 1-azahelicenes using easily available quinoline derivatives and cyclic diaryliodonium salts as starting materials. This reaction undergoes a palladium-catalyzed dual C-H activation/cyclization process to give facile access to a wide range of 1-aza[5]helicenes and 1-aza[6]helicenes with abundant functional groups (including F, Cl, Br, I, CF<sub>3</sub>, SeR, SR, and heteroaryl) in moderate to excellent yields, thereby providing new opportunities to fine-tune the properties of the helicene backbone. In addition, the obtained products could be further transformed into helicene-based Lewis base catalysts and redox switch materials easily. Notably, one selected 1-azahelicene shined bright yellow light by aggregation. These features enlarge the chemical space of 1-azahelicenes and inspire further utilization in other areas of research.

Organic LettersVol. 26(42)
Soochow University (CN)
National Natural Science Foundation of China, Priority Academic Program Development of Jiangsu Higher Education Institutions
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
1.25
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