Aerobic Oxidative Dethioacetalization Catalyzed by an Iron Phthalocyanine Complex

An aerobic oxidative dethioacetalization catalyzed by an iron octacarboxyphthalocyanine complex, which is designed by mimicking enzymatic oxidation, in an aqueous media is developed. The developed method can efficiently convert a broad range of dithioacetals, including those derived from aryl and aliphatic ketones and aldehydes, into the corresponding carbonyl compounds while tolerating various functional groups. This protocol is readily scalable to the gram scale. Mechanistic studies indicate that the iron phthalocyanine complex initiates the reaction by accepting a single electron from the sulfur atom of the dithioacetal, forming a radical cation intermediate. This is followed by unimolecular fragmentation and subsequent degradation of the resulting hemithioacetal to afford the corresponding carbonyl product, along with 1,2‐dithiolane and its oxides.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-11-26
DOI
https://doi.org/10.1002/adsc.70154
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Aerobic Oxidative Dethioacetalization Catalyzed by an Iron Phthalocyanine Complex

Ryo Sato, Hirofumi Ueda, Hidetoshi Tokuyama, Nagao Kobayashi et al.
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

Aerobic Oxidative Dethioacetalization Catalyzed by an Iron Phthalocyanine Complex

Ryo Sato, Hirofumi Ueda, Hidetoshi Tokuyama, Nagao Kobayashi, Hayato Machii
article en

Abstract

An aerobic oxidative dethioacetalization catalyzed by an iron octacarboxyphthalocyanine complex, which is designed by mimicking enzymatic oxidation, in an aqueous media is developed. The developed method can efficiently convert a broad range of dithioacetals, including those derived from aryl and aliphatic ketones and aldehydes, into the corresponding carbonyl compounds while tolerating various functional groups. This protocol is readily scalable to the gram scale. Mechanistic studies indicate that the iron phthalocyanine complex initiates the reaction by accepting a single electron from the sulfur atom of the dithioacetal, forming a radical cation intermediate. This is followed by unimolecular fragmentation and subsequent degradation of the resulting hemithioacetal to afford the corresponding carbonyl product, along with 1,2‐dithiolane and its oxides.

Advanced Synthesis & CatalysisVol. 368(2)
Tohoku University (JP)
Openalex Percentile: Top 72%
Catalytic C–H Functionalization Methods
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