BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Zhang W, Li H, Li X, Zou Z, Huang M, Liu J, Wang X, Ni S, Pan Y, Wang Y. A practical fluorosulfonylating platform via photocatalytic imidazolium-based SO2F radical reagent. Nat Commun 2022;13:3515. [PMID: 35717500 DOI: 10.1038/s41467-022-31296-2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Kong X, Chen Y, Liu Q, Wang W, Zhang S, Zhang Q, Chen X, Xu YQ, Cao ZY. Selective Fluorosulfonylation of Thianthrenium Salts Enabled by Electrochemistry. Org Lett 2023;25:581-6. [PMID: 36695525 DOI: 10.1021/acs.orglett.2c03956] [Reference Citation Analysis]
2 Erchinger JE, Hoogesteger R, Laskar R, Dutta S, Hümpel C, Rana D, Daniliuc CG, Glorius F. EnT-Mediated N-S Bond Homolysis of a Bifunctional Reagent Leading to Aliphatic Sulfonyl Fluorides. J Am Chem Soc 2023;145:2364-74. [PMID: 36652725 DOI: 10.1021/jacs.2c11295] [Reference Citation Analysis]
3 Zhang H, Yang N, Li J, Wang P, Li S, Xie L, Liao S. Radical Fluorosulfonyl Arylation of Alkenes: Accessing FSO2-Functionalized Chromanes via Formal Endo and Exo Cyclization. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03224] [Reference Citation Analysis]
4 Gu XT, Li LH, Wei Y, Shi M. Selective C(sp2)-H bond functionalization of olefins via visible-light-induced photoredox-quinuclidine dual catalysis. Chem Commun (Camb) 2022. [PMID: 35983765 DOI: 10.1039/d2cc03694k] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Cui Y, Zhao Y, Shen J, Zhang G, Ding C. The stable “F–SO2+” donor provides a mild and efficient approach to nitriles and amides. RSC Adv 2022;12:33064-33068. [DOI: 10.1039/d2ra05890a] [Reference Citation Analysis]
6 He F, Li Y, Wu J. Fluorosulfonyl radicals: new horizons for the synthesis of sulfonyl fluorides. Org Chem Front . [DOI: 10.1039/d2qo01211a] [Reference Citation Analysis]