Palladium‐Catalyzed Formal [4 + 2] Benzannulation of 1‐ferrocenyl‐2‐bromobenzene with Alkynes

Abstract A Pd‐catalyzed formal [4 + 2] benzannulation of 1‐ferrocenyl‐2‐bromobenzene with diarylacetylenes involving C─C coupling/C─H functionalization processes are developed, which provides a straightforward access to various substituted naphtho‐ferrocenes. This methodology offers a novel and efficient approach to produce polycyclic aromatic hydrocarbons (PAHs). The preliminary investigation shows the chiral phosphine ligand N ‐Me‐PC‐Phos has great potential in the asymmetric synthesis of planar naphtho‐ferrocene derivatives.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-08-19
DOI
https://doi.org/10.1002/ajoc.202500272
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

Palladium‐Catalyzed Formal [4 + 2] Benzannulation of 1‐ferrocenyl‐2‐bromobenzene with Alkynes

Wen‐Bo Li, Yin‐Lin Li, Peichao Zhang, Jiafeng He et al.
2 citations
Asian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
1.87
article

Palladium‐Catalyzed Formal [4 + 2] Benzannulation of 1‐ferrocenyl‐2‐bromobenzene with Alkynes

Wen‐Bo Li, Yin‐Lin Li, Peichao Zhang, Jiafeng He, Lu Liu
article en
2 citations

Abstract

Abstract A Pd‐catalyzed formal [4 + 2] benzannulation of 1‐ferrocenyl‐2‐bromobenzene with diarylacetylenes involving C─C coupling/C─H functionalization processes are developed, which provides a straightforward access to various substituted naphtho‐ferrocenes. This methodology offers a novel and efficient approach to produce polycyclic aromatic hydrocarbons (PAHs). The preliminary investigation shows the chiral phosphine ligand N ‐Me‐PC‐Phos has great potential in the asymmetric synthesis of planar naphtho‐ferrocene derivatives.

Asian Journal of Organic ChemistryVol. 14(10)
East China Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Catalytic C–H Functionalization Methods
1.87
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