Similar Publications

Photoinduced Cross-Coupling of Trifluoromethylarenes with Heteroarenes via Unactivated C(sp)-F and C(sp)-H Selective Cleavage.

Org Lett

January 2025

Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710127, China.

The installation of -difluoromethylene groups into two adjacent aryl groups is a formidable synthetic challenge despite their attractive structural, physical, and biochemical properties. Herein, we disclose a photoredox-catalyzed selective defluoroarylation of heteroarenes through inert C(sp)-F and C(sp)-H selective cleavage, which provides a straightforward route to access medicinally relevant aryl-heteroaryl or heteroaryl-heteroaryl difluoromethane scaffolds. Salient features of this reaction include readily accessible starting materials, metal-free conditions, and broad substrate scope.

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Photoredox-catalyzed phosphonylation of bromo-substituted 1,10-phenanthrolines under visible light irradiation was studied. The reaction was shown to proceed under mild conditions with Eosin Y as a photocatalyst in DMSO under blue light irradiation. It is transition-metal-free and affords the target phosphonate-substituted 1,10-phenanthrolines in moderate yields (26-51%) in 22 to 40 h.

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In this study, we present a groundbreaking approach utilizing metal-free, visible light-mediated organic photoredox catalyzed atom transfer radical polymerization (O-ATRP) to synthesize cellulose-based stimuli-responsive polymers. Our method resulted in the successful synthesis of innovative metal-free poly(N-tertiary-butylacrylamide)-graft-hydroxypropyl cellulose (PNTBAM-g-HPC) polymers with exceptional control over molecular weight and narrow dispersity index (Đ) and explored their applications in organo-photocatalytic reactions. This approach addresses the limitations of traditional atom transfer radical polymerization method, which suffer from metal contamination and toxicity related problems.

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Photoredox-Catalyzed Three-Component Construction of Aryl Sulfonyl Fluoride Using KHF: Late-Stage Drug Fluorosulfonylation.

J Org Chem

November 2024

Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education, School of Chemistry and Materials Science, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.

Article Synopsis
  • Aryl sulfonyl fluorides are important in organic synthesis and medicinal chemistry, and a new metal-free method using photoredox catalysis for their production has been developed.
  • The process involves a three-component reaction using aryl sulfonyl ammonium salts and dibenzothiophenium salts, employing KHF as the fluorine source to create diverse aryl sulfonyl fluorides under mild conditions.
  • This method yields good results and is efficient for drug fluorosulfonylation, showcasing versatility and the ability to modify these compounds for further applications.
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Organic Photoredox-Catalyzed Hydrosilylation of Vinylboronic Esters for the Synthesis of Geminal and Vicinal Borosilanes.

J Org Chem

November 2024

Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002, China.

Geminal and vicinal borosilanes have unique applications in functional materials and synthetic transformations. Herein, a convenient method for the synthesis of geminal and vicinal borosilanes is developed via photoredox metal-free hydrosilylation of vinylboronic esters. This strategy features the advantages of high atom economy, environmental friendliness, and excellent functional group compatibility.

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