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For: Wolf R, Orni-wasserlauf R. A century of the synthesis of dapsone: its anti-infective capacity now and then. Int J Dermatol 2000;39:779-83. [DOI: 10.1046/j.1365-4362.2000.00739.x] [Cited by in Crossref: 21] [Cited by in F6Publishing: 16] [Article Influence: 1.0] [Reference Citation Analysis]
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8 Schneider-Rauber G, Argenta DF, Caon T. Emerging Technologies to Target Drug Delivery to the Skin - the Role of Crystals and Carrier-Based Systems in the Case Study of Dapsone. Pharm Res 2020;37:240. [PMID: 33169237 DOI: 10.1007/s11095-020-02951-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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13 Lemmer H, Stieger N, Liebenberg W, Caira MR. Solvatomorphism of the Antibacterial Dapsone: X-ray Structures and Thermal Desolvation Kinetics. Crystal Growth & Design 2012;12:1683-92. [DOI: 10.1021/cg300019f] [Cited by in Crossref: 26] [Cited by in F6Publishing: 13] [Article Influence: 2.9] [Reference Citation Analysis]
14 Braun DE, Krüger H, Kahlenberg V, Griesser UJ. Molecular Level Understanding of the Reversible Phase Transformation between Forms III and II of Dapsone. Cryst Growth Des 2017;17:5054-60. [PMID: 30337848 DOI: 10.1021/acs.cgd.7b01089] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 3.3] [Reference Citation Analysis]
15 Dodds AC, Sutherland A. Regioselective C-H Thioarylation of Electron-Rich Arenes by Iron(III) Triflimide Catalysis. J Org Chem 2021;86:5922-32. [PMID: 33783222 DOI: 10.1021/acs.joc.1c00448] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Gonzalez-Benavides N, Vera-Cabrera L, Sanchez-Meza E, Ocampo-Candiani J, Welsh O. Diaminodiphenyl-sulphone: in vitro activity alone and in combination with other antimicrobials against 30 strains of Nocardia brasiliensis. J Eur Acad Dermatol Venereol 2019;33:e395-6. [PMID: 31063602 DOI: 10.1111/jdv.15660] [Cited by in F6Publishing: 1] [Reference Citation Analysis]