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For: Mondal S, Malakar S. Synthesis of sulfonamide and their synthetic and therapeutic applications: Recent advances. Tetrahedron 2020;76:131662. [DOI: 10.1016/j.tet.2020.131662] [Cited by in Crossref: 14] [Cited by in F6Publishing: 1] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Tekin S, Karatay A, Erdener D, Yildiz EA, Boyacioglu B, Ünver H, Yıldız M, Elmalı A. Colorimetric probe and optical behaviours of new azomethine derivatives of sulfonamide. Journal of Molecular Structure 2022;1253:132239. [DOI: 10.1016/j.molstruc.2021.132239] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Radchenko OB, Radchenko DS, Konovets AI, Grygorenko OO. Water Determination in Aromatic Sulfonyl Chlorides Using the Karl Fischer Titration Method: Scope and Limitations. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202102749] [Reference Citation Analysis]
3 Wu P, Ren H. Azobenzene with sulfonamide group deprotonated by green developer for moisture detection and water jet rewritable paper. Dyes and Pigments 2021;196:109764. [DOI: 10.1016/j.dyepig.2021.109764] [Reference Citation Analysis]
4 Sang D, Dong B, Liu Y, Tian J. Chemoselective Cleavage of Acylsulfonamides and Sulfonamides by Aluminum Halides. J Org Chem 2022. [PMID: 35157468 DOI: 10.1021/acs.joc.1c03133] [Reference Citation Analysis]
5 Tilby MJ, Dewez DF, Pantaine LRE, Hall A, Martínez-Lamenca C, Willis MC. Photocatalytic Late-Stage Functionalization of Sulfonamides via Sulfonyl Radical Intermediates. ACS Catal 2022;12:6060-7. [PMID: 35633900 DOI: 10.1021/acscatal.2c01442] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Adamovich SN, Ushakov IA, Oborina EN, Vashchenko AV. Silatrane-sulfonamide hybrids: Synthesis, characterization, and evaluation of biological activity. Journal of Organometallic Chemistry 2022;957:122150. [DOI: 10.1016/j.jorganchem.2021.122150] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Yildiz EA, Tekin S, Erdener D, Karatay A, Boyacioglu B, Ünver H, Yıldız M, Elmali A. Naked-eye colorimetric anion probing and fluorescent switching features of conjugated Schiff Bases derived from 4-(Trifluoromethyl) benzenesulfonamide. Journal of Luminescence 2022;247:118849. [DOI: 10.1016/j.jlumin.2022.118849] [Reference Citation Analysis]
8 Zhang Z, Willis MC. Sulfondiimidamides as new functional groups for synthetic and medicinal chemistry. Chem 2022. [DOI: 10.1016/j.chempr.2022.02.013] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
9 Fantacuzzi M, Amoroso R, Carradori S, De Filippis B. Resveratrol-based compounds and neurodegeneration: Recent insight in multitarget therapy. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114242] [Reference Citation Analysis]
10 de Faria LV, Lisboa TP, Campos NDS, Alves GF, Matos MAC, Matos RC, Munoz RAA. Electrochemical methods for the determination of antibiotic residues in milk: A critical review. Anal Chim Acta 2021;1173:338569. [PMID: 34172150 DOI: 10.1016/j.aca.2021.338569] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Zhao W, Zheng S, Zou J, Liang Y, Zhao C, Xu H. Synthesis of Novel Pesticidal N,N'-Disubstituted Sulfamide Derivatives Using Sulfur(VI) Fluorine Exchange Click Reaction. J Agric Food Chem 2021;69:5798-803. [PMID: 34028259 DOI: 10.1021/acs.jafc.0c04194] [Reference Citation Analysis]
12 Liu H, Zhang B, Zhao W, Yu X, Zhu W, Xia C, Zhou Y. Base-Mediated Coupling Reactions of Benzenesulfonyl Azides with Proline: Synthesis of Proline-Derived Benzenesulfonamides. ACS Omega 2021;6:34796-804. [PMID: 34963962 DOI: 10.1021/acsomega.1c05331] [Reference Citation Analysis]
13 Gevondian AG, Kotovshchikov YN, Latyshev GV, Lukashev NV, Beletskaya IP. Domino Construction of Benzoxazole-Derived Sulfonamides via Metal-Free Denitrogenation of 5-Iodo-1,2,3-triazoles in the Presence of SO2 and Amines. J Org Chem 2021;86:5639-50. [PMID: 33822625 DOI: 10.1021/acs.joc.1c00115] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
14 Bredael K, Geurs S, Clarisse D, De Bosscher K, D’hooghe M, Trabocchi A. Carboxylic Acid Bioisosteres in Medicinal Chemistry: Synthesis and Properties. Journal of Chemistry 2022;2022:1-21. [DOI: 10.1155/2022/2164558] [Reference Citation Analysis]
15 Kim DS, Lee HG. Formation of the Tertiary Sulfonamide C(sp3)-N Bond Using Alkyl Boronic Ester via Intramolecular and Intermolecular Copper-Catalyzed Oxidative Cross-Coupling. J Org Chem 2021;86:17380-94. [PMID: 34762422 DOI: 10.1021/acs.joc.1c01759] [Reference Citation Analysis]
16 Mondal S. Sulfonamide synthesis under green conditions. Synthetic Communications 2021;51:1023-44. [DOI: 10.1080/00397911.2020.1870238] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
17 Andriashvili VA, Zhersh S, Tolmachev AA, Grygorenko OO. Synthesis of α-C-Stereochemically Pure Secondary Sulfonamides. J Org Chem 2022. [PMID: 35441519 DOI: 10.1021/acs.joc.2c00480] [Reference Citation Analysis]
18 Siddiqui WA, Khalid M, Ashraf A, Shafiq I, Parvez M, Imran M, Irfan A, Hanif M, Khan MU, Sher F, Ali A. Antibacterial metal complexes of o ‐sulfamoylbenzoic acid: Synthesis, characterization, and DFT study. Applied Organom Chemis 2022;36. [DOI: 10.1002/aoc.6464] [Reference Citation Analysis]
19 Padma Priya V, Natarajan K, Nandi GC. Advances in the photoredox catalysis of S(VI) compounds. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132711] [Reference Citation Analysis]
20 Liu TL, Jhou ML, Hsieh CE, Lin CJ, Su HH, Chou CM. Palladium-Catalyzed Intramolecular Allylic Amidation via Decarboxylative Aromatization: Synthesis of N-Allyl-N-aryl Sulfonamides. J Org Chem 2021;86:9084-95. [PMID: 34115505 DOI: 10.1021/acs.joc.1c01065] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]