Versatile Metal‐Free Arylation of BODIPY and Bis(BF₂) Chromophores by Using Arylazosulfones in a Sunflow System

Chemistry - A European Journal, Год журнала: 2024, Номер 30(61)

Опубликована: Июль 30, 2024

Abstract BODIPYs have a well‐established role in biological sciences as chemosensors and versatile markers due to their chemical reactivity, which allows for fine‐tuning of photophysical characteristics. In this work, we combined the unique reactivity arylazo sulfones with advantages “sunflow” reactor develop fast, efficient, method photochemical arylation other chromophores. This approach resulted red‐shifted emitting fluorophores extended electronic delocalization at 3‐ 5‐positions BODIPY core. represents an advantageous functionalization compared existing strategies.

Язык: Английский

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Visible-light-promoted selenylation/cyclization of o-(1-alkynyl) benzoates to access seleno-substituted isocoumarins

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(36), С. 7327 - 7331

Опубликована: Янв. 1, 2024

A simple and efficient method to access 4-selenyl-isocoumarin derivatives through visible-light-promoted selenylation/cyclization of o -(1-alkynyl) benzoates has been developed.

Язык: Английский

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Visible‐Light Enabled Synthesis of 1‐Aryl‐3‐Sulfonylmethyl‐1,2,4‐Triazoles by Arylazo Sulfones

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 5, 2024

Abstract We present a novel and highly efficient method for synthesizing polyfunctionalized 1,2,4‐triazoles. This approach leverages visible light arylazo sulfones in combination with N ‐vinyl amides, the environmentally friendly solvent ethyl acetate. Remarkably, reaction proceeds without need (photo)catalysts, ensuring near‐perfect atom economy producing only water as by‐product. exhibits excellent functional group tolerance can be scaled both batch continuous‐flow processes.

Язык: Английский

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