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Cited by in F6Publishing
For: Ye X, Wu X, Guo S, Huang D, Sun X. Recent advances of sodium sulfinates in radical reactions. Tetrahedron Letters 2021;81:153368. [DOI: 10.1016/j.tetlet.2021.153368] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Renzi P, Azzi E, Ascensio S, Parisotto S, Sordello F, Pellegrino F, Ghigo G, Deagostino A. Inexpensive and bench stable diarylmethylium tetrafluoroborates as organocatalysts in the light mediated hydrosulfonylation of unactivated alkenes. Chem Sci 2023;14:2721-34. [PMID: 36908942 DOI: 10.1039/d3sc00182b] [Reference Citation Analysis]
2 Peng P, Yang R, Xu B. Tunable Reduction of Benzyl α , α ‐Difluorotriflones: Synthesis of Difluoroarenes and Sodium Aryldifluoromethyl Sufinates and their Applications. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202202870] [Reference Citation Analysis]
3 Li W, Chen X, Zhou L. Photocatalytic Defluorinative Three-Component Reaction of α-Trifluoromethyl Alkenes, Alkenes, and Sodium Sulfinates: Synthesis of Monofluorocyclopentenes. Org Lett 2022. [PMID: 35926080 DOI: 10.1021/acs.orglett.2c02202] [Reference Citation Analysis]
4 Mou XQ, Ren LC, Zhang M, Wang M, Jin YF, Guan QX, Cai A, Zhang SM, Ren H, Zhang Y, Chen YZ. Complementary Copper-Catalyzed and Electrochemical Aminosulfonylation of O-Homoallyl Benzimidates and N-Alkenyl Amidines with Sodium Sulfinates. Org Lett 2022. [PMID: 35138858 DOI: 10.1021/acs.orglett.2c00287] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Gladkov AA, Chernov GN, Levin VV, Kokorekin VA, Dilman AD. Photoredox Activation of Organozinc Reagents: Barbier-Type Reaction of Alkyl Halides with α-(Trifluoromethyl)styrenes. Org Lett 2021;23:9645-8. [PMID: 34818011 DOI: 10.1021/acs.orglett.1c03917] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
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