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Cited by in F6Publishing
For: Lam LY, Ma C. Chan-Lam-Type C-S Coupling Reaction by Sodium Aryl Sulfinates and Organoboron Compounds. Org Lett 2021;23:6164-8. [PMID: 34292759 DOI: 10.1021/acs.orglett.1c02299] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Yu X, Wei W, Niu Y, Li X, Wang M, Gao W. Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides. Molecules 2022;27:6232. [DOI: 10.3390/molecules27196232] [Reference Citation Analysis]
2 Li XY, Liu Y, Yu B. Nucleophilic Addition/Electrocyclization Strategy toward Polyheterocyclic-Fused Quinoline-2-thiones in Green Solvent. J Org Chem 2022. [PMID: 36094161 DOI: 10.1021/acs.joc.2c00893] [Reference Citation Analysis]
3 Lam LY, Chan KH, Ma C. Copper-Catalyzed Synthesis of Functionalized Aryl Sulfonamides from Sodium Sulfinates in Green Solvents. J Org Chem 2022. [PMID: 35723444 DOI: 10.1021/acs.joc.2c00777] [Reference Citation Analysis]
4 Bose S, Dutta S, Koley D. Entering Chemical Space with Theoretical Underpinning of the Mechanistic Pathways in the Chan–Lam Amination. ACS Catal 2022;12:1461-74. [DOI: 10.1021/acscatal.1c04479] [Cited by in F6Publishing: 1] [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: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]