Pd-Catalyzed Dearomative Functionalizations of Benzyl and Aryl Electrophiles

Dearomative functionalization is a powerful method to construct structurally complex alicyclic frameworks from simple and abundant aromatic molecules. Although a myriad of dearomative functionalizations have been reported so far, the reaction of electron-neutral arenes such as benzenes and naphthalenes are a still challenging issue due to their high aromatic stability, often requiring an excess amount of aromatic starting materials. Recently, we have developed catalytic dearomative functionalization of electron-neutral arenes by focusing on the unique reactivity of π-benzyl palladium catalysis. In this manuscript, we describe our endeavor to develop the dearomative C-C bond formations of benzyl alcohol derivatives, benzyl ammoniums, and bromoarenes. The dearomatized compound was transformed into various alicyclic skeletons by diverse derivatizations. Furthermore, we successfully achieved dearomative C-N bond formation with bromo(hetero)arenes, resulting in the synthesis of azaspirocycles. Utilizing the present methodology, the total synthesis of Cephalotaxus alkaloids with a unique complex polycyclic skeleton, has also been accomplished.

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Journal
Journal of Synthetic Organic Chemistry Japan
Published
2024-10-01
DOI
https://doi.org/10.5059/yukigoseikyokaishi.82.965
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
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article

Pd-Catalyzed Dearomative Functionalizations of Benzyl and Aryl Electrophiles

Hiroki Kato, Junichiro Yamaguchi, Kei Muto
Journal of Synthetic Organic Chemistry Japan
Cyclopropane Reaction Mechanisms
article

Pd-Catalyzed Dearomative Functionalizations of Benzyl and Aryl Electrophiles

Hiroki Kato, Junichiro Yamaguchi, Kei Muto
article en

Abstract

Dearomative functionalization is a powerful method to construct structurally complex alicyclic frameworks from simple and abundant aromatic molecules. Although a myriad of dearomative functionalizations have been reported so far, the reaction of electron-neutral arenes such as benzenes and naphthalenes are a still challenging issue due to their high aromatic stability, often requiring an excess amount of aromatic starting materials. Recently, we have developed catalytic dearomative functionalization of electron-neutral arenes by focusing on the unique reactivity of π-benzyl palladium catalysis. In this manuscript, we describe our endeavor to develop the dearomative C-C bond formations of benzyl alcohol derivatives, benzyl ammoniums, and bromoarenes. The dearomatized compound was transformed into various alicyclic skeletons by diverse derivatizations. Furthermore, we successfully achieved dearomative C-N bond formation with bromo(hetero)arenes, resulting in the synthesis of azaspirocycles. Utilizing the present methodology, the total synthesis of Cephalotaxus alkaloids with a unique complex polycyclic skeleton, has also been accomplished.

Journal of Synthetic Organic Chemistry JapanVol. 82(10)
Waseda University (JP)
Openalex Percentile: Top 87%
Cyclopropane Reaction Mechanisms
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Pd-Catalyzed Dearomative Functionalizations of Benzyl and Aryl Electrophiles — Hiroki Kato, Junichiro Yamaguchi, et al. · Journal of Synthetic Organic Chemistry Japan (2024) | TGRS Research Map | TGRS