Study on the development of radical building block: Mn(III)-based reaction of 1,3-indanedione

The Mn(III)-based oxidation of 1,3-indanedione (1) with 1,1-diarylethenes 2a–c effectively proceeded in boiling AcOH to produce 2,2-bis(vinyl)indanediones 5a–c and 1,2'-spirobi[indene]-1',3'-diones 6a–c via the formation of 2,2-bis(2-acetoxyethyl)indanedione 3 and acetoxyindeno[1,2-b]furan-4-one 4 intermediates. On the other hand, the Mn(III)-based aerobic oxidation of 1a with 2a at room temperature resulted in bis(endoperoxide) 8a and endoperoxypropellane 9a via the production of mono(endoperoxide) 7a. The plausible reaction pathways were also discussed.

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Publication Details

Journal
Synthetic Communications
Published
2024-08-09
DOI
https://doi.org/10.1080/00397911.2024.2385542
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Study on the development of radical building block: Mn(III)-based reaction of 1,3-indanedione

Kazuki Hisano, Hiroshi Nishino
Synthetic Communications
Oxidative Organic Chemistry Reactions
article

Study on the development of radical building block: Mn(III)-based reaction of 1,3-indanedione

Kazuki Hisano, Hiroshi Nishino
article en

Abstract

The Mn(III)-based oxidation of 1,3-indanedione (1) with 1,1-diarylethenes 2a–c effectively proceeded in boiling AcOH to produce 2,2-bis(vinyl)indanediones 5a–c and 1,2'-spirobi[indene]-1',3'-diones 6a–c via the formation of 2,2-bis(2-acetoxyethyl)indanedione 3 and acetoxyindeno[1,2-b]furan-4-one 4 intermediates. On the other hand, the Mn(III)-based aerobic oxidation of 1a with 2a at room temperature resulted in bis(endoperoxide) 8a and endoperoxypropellane 9a via the production of mono(endoperoxide) 7a. The plausible reaction pathways were also discussed.

Synthetic CommunicationsVol. 54(16)
Kumamoto University (JP)
Japan Society for the Promotion of Science
Sustainable cities and communities
Openalex Percentile: Top 91%
Oxidative Organic Chemistry Reactions
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