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For: Lai J, Yuan G. A novel synthesis of aryl methyl sulfones and β -hydroxysulfones from sodium sulfinates and di -tert -butyl peroxide in H 2 O medium. Tetrahedron Letters 2018;59:524-7. [DOI: 10.1016/j.tetlet.2017.12.074] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Son S, Shyam PK, Park H, Jeong I, Jang H. Complementary Strategy for Regioselective Synthesis of Diverse β-Hydroxysulfones from Thiosulfonates: Complementary Strategy for Regioselective Synthesis of Diverse β-Hydroxysulfones from Thiosulfonates. Eur J Org Chem 2018;2018:3365-71. [DOI: 10.1002/ejoc.201800778] [Cited by in Crossref: 12] [Article Influence: 3.0] [Reference Citation Analysis]
2 Lanfranco A, Moro R, Azzi E, Deagostino A, Renzi P. Unconventional approaches for the introduction of sulfur-based functional groups. Org Biomol Chem 2021;19:6926-57. [PMID: 34333579 DOI: 10.1039/d1ob01091c] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Liu C, Yang Y, Dong J, Zhou M, Li L, Wang H. Visible-light-promoted hydroxysulfonylation of alkylidenecyclopropanes: synthesis of cyclopropane-containing β-hydroxysulfones. Org Chem Front 2019;6:3944-9. [DOI: 10.1039/c9qo01058k] [Cited by in Crossref: 6] [Article Influence: 2.0] [Reference Citation Analysis]
4 Reddy RJ, Kumari AH. Synthesis and applications of sodium sulfinates (RSO 2 Na): a powerful building block for the synthesis of organosulfur compounds. RSC Adv 2021;11:9130-221. [DOI: 10.1039/d0ra09759d] [Cited by in Crossref: 20] [Cited by in F6Publishing: 5] [Article Influence: 20.0] [Reference Citation Analysis]
5 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: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]