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For: Mustafa M, Winum JY. The importance of sulfur-containing motifs in drug design and discovery. Expert Opin Drug Discov 2022;:1-12. [PMID: 35193437 DOI: 10.1080/17460441.2022.2044783] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Vennila P, Al-otaibi JS, Venkatesh G, Sheena Mary Y, Raj V, Acharjee N, Tamilselvi P. Structural, Spectral, Molecular Docking, and Molecular Dynamics Simulations of Phenylthiophene-2-Carboxylate Compounds as Potential Anticancer Agents. Polycyclic Aromatic Compounds 2023. [DOI: 10.1080/10406638.2023.2172052] [Reference Citation Analysis]
2 Du G, Zhu P, Wang J, Li X, Zhang D, Wang C, Sun F. Modular Synthesis of ortho ‐Thiolated Aryl Esters Enabled with Thiocarbonate through Catellani Strategy. Eur J Org Chem 2023. [DOI: 10.1002/ejoc.202201382] [Reference Citation Analysis]
3 Yang Z, Sun X, Jin D, Qiu Y, Chen L, Sun L, Gu W. Novel Camphor Sulfonohydrazide and Sulfonamide Derivatives as Potential Succinate Dehydrogenase Inhibitors against Phytopathogenic Fungi/Oomycetes. J Agric Food Chem 2023;71:174-85. [PMID: 36562624 DOI: 10.1021/acs.jafc.2c05628] [Reference Citation Analysis]
4 Gao S, Song L, Cheng Y, Zhao F, Kang D, Song S, Yang M, Ye B, Zhao W, Tang Y, De Clercq E, Pannecouque C, Zhan P, Liu X. Discovery of novel sulfonamide substituted indolylarylsulfones as potent HIV-1 inhibitors with better safety profiles. Acta Pharmaceutica Sinica B 2023. [DOI: 10.1016/j.apsb.2023.01.003] [Reference Citation Analysis]
5 Mor S, Sindhu S, Khatri M, Punia R, Jakhar K. Synthesis, Type II diabetes inhibitory activity, antimicrobial evaluation, and docking studies of N'-arylidene-2-((7-methylbenzo[4,5]thiazolo[2,3-c] [1,2,4]triazol-3-yl)thio)acetohydrazides. Eur J Chem 2022;13:426-434. [DOI: 10.5155/eurjchem.13.4.426-434.2315] [Reference Citation Analysis]
6 Mondal S, Di Tommaso EM, Olofsson B. Transition-Metal-Free Difunctionalization of Sulfur Nucleophiles. Angew Chem Int Ed Engl 2022;:e202216296. [PMID: 36546892 DOI: 10.1002/anie.202216296] [Reference Citation Analysis]
7 Abdiaj I, Cañellas S, Dieguez A, Linares ML, Pijper B, Fontana A, Rodriguez R, Trabanco A, Palao E, Alcázar J. End-to-End Automated Synthesis of C(sp(3))-Enriched Drug-like Molecules via Negishi Coupling and Novel, Automated Liquid-Liquid Extraction. J Med Chem 2023;66:716-32. [PMID: 36520521 DOI: 10.1021/acs.jmedchem.2c01646] [Reference Citation Analysis]
8 Zhong Z, Chesti J, Armstrong A, Bull JA. Synthesis of Sulfoximine Propargyl Carbamates under Improved Conditions for Rhodium Catalyzed Carbamate Transfer to Sulfoxides. J Org Chem 2022;87:16115-26. [PMID: 36379008 DOI: 10.1021/acs.joc.2c02083] [Reference Citation Analysis]
9 Iyer MR, Bhattacharjee P, Kundu B, Rutland N, Wood CM. One-Pot Synthesis of Thio-Augmented Sulfonylureas via a Modified Bunte’s Reaction. ACS Omega. [DOI: 10.1021/acsomega.2c04816] [Reference Citation Analysis]
10 Lücking U. New Opportunities for the Utilization of the Sulfoximine Group in Medicinal Chemistry from the Drug Designer's Perspective**. Chemistry A European J 2022. [DOI: 10.1002/chem.202201993] [Reference Citation Analysis]
11 Terhorst S, Jansen T, Langletz T, Bolm C. Sulfonimidamides by Sequential Mechanochemical Chlorinations and Aminations of Sulfinamides. Org Lett 2022. [PMID: 35658444 DOI: 10.1021/acs.orglett.2c01099] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Passia MT, Schöbel JH, Bolm C. Sulfondiimines: synthesis, derivatisation and application. Chem Soc Rev 2022. [PMID: 35616027 DOI: 10.1039/d2cs00098a] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]