Synthesis of 1,4‐Naphthoquinones via Palladium(II)‐Catalyzed Tertiary C−H Alkylation of Olefins Followed by C−C Bond Cleavage

Abstract An efficient method has been developed for the preparation of 1,4‐naphthoquinones via a palladium‐catalyzed reaction of 2‐aryl‐1,3‐indandiones with olefins. This reaction involves the tertiary C−H alkylation of 2‐aryl‐1,3‐indandiones with olefins to produce a tertiary alcohol, followed by C−C bond cleavage.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-11-28
DOI
https://doi.org/10.1002/ejoc.202401107
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of 1,4‐Naphthoquinones via Palladium(II)‐Catalyzed Tertiary C−H Alkylation of Olefins Followed by C−C Bond Cleavage

Mengfan Chang, Ting Li, Wenguang Li, Xu Zhang et al.
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

Synthesis of 1,4‐Naphthoquinones via Palladium(II)‐Catalyzed Tertiary C−H Alkylation of Olefins Followed by C−C Bond Cleavage

Mengfan Chang, Ting Li, Wenguang Li, Xu Zhang, Xuefeng Xu, Tongtong Ni
article en

Abstract

Abstract An efficient method has been developed for the preparation of 1,4‐naphthoquinones via a palladium‐catalyzed reaction of 2‐aryl‐1,3‐indandiones with olefins. This reaction involves the tertiary C−H alkylation of 2‐aryl‐1,3‐indandiones with olefins to produce a tertiary alcohol, followed by C−C bond cleavage.

European Journal of Organic ChemistryVol. 28(4)
Nanyang Normal University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 84%
Catalytic C–H Functionalization Methods
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