Abstract
AbstractSulfonyl and sulfonimidoyl fluorides are versatile substrates in organic synthesis and medicinal chemistry. However, they have been exclusively used as S(VI)+ electrophiles for defluorinative ligations. Converting sulfonyl and sulfonimidoyl fluorides to S(VI) radicals is challenging and underexplored due to the strong bond dissociation energy of SVI−F and high reduction potentials, but once achieved would enable dramatically expanded synthetic utility and downstream applications. In this report, we disclose a general platform to address this issue through cooperative organosuperbase activation and photoredox catalysis. Vinyl sulfones and sulfoximines are obtained with excellent E selectivity under mild conditions by coupling reactions with alkenes. The synthetic utility of this method in the preparation of functional polymers and dyes is also demonstrated.
Funder
National Natural Science Foundation of China
Science and Technology Foundation of Hunan Province
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary
Reference92 articles.
1. Takacs, G. A. Heats of formation and bond dissociation energies of some simple sulfur- and halogen-containing molecules. J. Chem. Eng. Data. 23, 174–175 (1978).
2. Salaudeen, B. Electrochemical reduction of arene sulfonyl fluorides and arene sulfonyl succinimides and their potential use as precursors for surface modification. (University of Guelph, 2020).
3. Parsons, J. S. Analysis of sulfonic acids by forming sulfonyl fluoride derivatives. J. Chromatogr. Sci. 5, 254–256 (1967).
4. Ciuffarin, E., Senatore, L. & Isola, M. Nucleophilic substitution at four-co-ordinate sulphur. Mobility of the leaving group. J. Chem. Soc., Perkin Trans. 2 4, 468–471 (1972).
5. Kice, J. L. & Lunney, E. A. Catalysis of the hydrolysis of aryl sulfonyl fluorides by acetate ion and triethylamine. J. Org. Chem. 40, 2125–2127 (1975).
Cited by
12 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献