Recent advances in photochemical and electrochemical strategies for the synthesis of sulfonyl fluorides
Literature Information
Publication Date
2023-11-14
DOI
10.1039/D3QO01610B
Impact Factor
5.281
Authors
Yu Zheng, Wenguang Lu, Tianting Ma, Shenlin Huang
View Original
Abstract
Sulfonyl fluorides display unique reactivity in organic synthesis and have wide applications in drug discovery, chemical biology, and materials science. Against the backdrop of increasing demands for environmental friendliness and sustainability, photochemical and electrochemical strategies have recently emerged as alternative methods for synthesizing diverse sulfonyl fluorides. This review highlights the recent advancements in these strategies, emphasizing their novel features and proposed mechanisms. We expect this review to inspire additional novel approaches to access diverse sulfonyl fluorides.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
Recommended Compounds
N-Methyl-3-(1-naphthyloxy)-3-(2-thienyl)-1-propanamine hydrochloride (1:1)
CAS Number:
1188266-11-6
Molecular Formula:
C18H20ClNOS
(3alpha,5beta,6alpha,7alpha)-6-Ethylcholane-3,7,24-triol
CAS Number:
1537866-49-1
Molecular Formula:
C26H46O3
Benzyl 6-oxo-3,6-dihydro-1(2H)-pyridinecarboxylate
CAS Number:
725746-35-0
Molecular Formula:
C13H13NO3
![1-oxaspiro[4.4]nonan-6-one structure](https://static.chemtradehub.com/structs/134/134179-01-4-e051.webp "1-oxaspiro[4.4]nonan-6-one structure")
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