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For: Sathiyaraj S, Shanavas A, Kumar KA, Sathiyaseelan A, Senthilselvan J, Kalaichelvan P, Nasar AS. The first example of bis(indolyl)methane based hyperbranched polyurethanes: Synthesis, solar cell application and anti-bacterial and anti-oxidant properties. European Polymer Journal 2017;95:216-31. [DOI: 10.1016/j.eurpolymj.2017.08.021] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Banari H, Kiyani H, Pourali AR. Bisindolization Reaction Employing Phthalimide-N-sulfonic Acid as an Efficient Catalyst. COCAT 2020;7:124-33. [DOI: 10.2174/2213337206666191022110730] [Reference Citation Analysis]
2 Ravivarma M, Kumar KA, Rajakumar P, Pandurangan A. Interfacial charge transport studies and fabrication of high performance DSSC with ethylene cored unsymmetrical dendrimers as quasi electrolytes. Journal of Molecular Liquids 2018;265:717-26. [DOI: 10.1016/j.molliq.2018.05.119] [Cited by in Crossref: 12] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
3 Singh A, Kaur G, Kaur A, Gupta VK, Banerjee B. A General Method for the Synthesis of 3,3-bis(indol-3-yl)indolin-2-ones, bis(indol-3-yl)(aryl)methanes and tris(indol-3-yl)methanes Using Naturally Occurring Mandelic Acid as an Efficient Organo-catalyst in Aqueous Ethanol at Room Temperature. CGC 2020;7:128-40. [DOI: 10.2174/2213346107666200228125715] [Cited by in Crossref: 13] [Cited by in F6Publishing: 4] [Article Influence: 6.5] [Reference Citation Analysis]
4 Li X, İlk S, Liu Y, Raina DB, Demircan D, Zhang B. Nonionic nontoxic antimicrobial polymers: indole-grafted poly(vinyl alcohol) with pendant alkyl or ether groups. Polym Chem 2022;13:2307-19. [DOI: 10.1039/d1py01504d] [Reference Citation Analysis]
5 Kadu VD, Patil AA, Shendage PR. Oxone-Promoted Synthesis of Bis(indolyl)methanes from Arylmethylamines and Indoles. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.133502] [Reference Citation Analysis]
6 Ali BM, Kumar KA, Sultan Nasar A. Fifth Generation Polyurethane Dendrimers Decorated with Protected Amine, Free Amine and Blocked Isocyanate End Groups: Synthesis and Electrolytic Performance to Increase the Efficiency of Dye‐Sensitized Solar Cell. ChemistrySelect 2019;4:12983-91. [DOI: 10.1002/slct.201903289] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Bargathulla I, Aadhil Ashwaq B, Sathiyaraj S, Sultan Nasar A, Elangovanvellaichamy. Pegylated bis-indolyl polyurethane dendrimer: Empty drug carrier with prominent anticancer activity. European Polymer Journal 2021;153:110491. [DOI: 10.1016/j.eurpolymj.2021.110491] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Singh A, Kaur G, Banerjee B. Recent Developments on the Synthesis of Biologically Significant bis/tris(indolyl)methanes under Various Reaction Conditions: A Review. COC 2020;24:583-621. [DOI: 10.2174/1385272824666200228092752] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 4.5] [Reference Citation Analysis]
9 Ahmadi Y, Siddiqui MT, Haq QMR, Ahmad S. Synthesis and characterization of surface-active antimicrobial hyperbranched polyurethane coatings based on oleo-ethers of boric acid. Arabian Journal of Chemistry 2020;13:2689-701. [DOI: 10.1016/j.arabjc.2018.07.001] [Cited by in Crossref: 11] [Cited by in F6Publishing: 2] [Article Influence: 5.5] [Reference Citation Analysis]
10 Qiang W, Liu X, Loh T. Supported Iridium Catalyst for the Green Synthesis of 3,3′-Bis(indolyl)methanes Using Methanol As the Bridging Methylene Source. ACS Sustainable Chem Eng 2019;7:8429-39. [DOI: 10.1021/acssuschemeng.9b00094] [Cited by in Crossref: 12] [Article Influence: 4.0] [Reference Citation Analysis]
11 Bargathulla I, Manivannan N, Gopinath A, Mathivanan N, Nasar AS. High density star poly HEMA containing bis-indole rich dendrimer inner core for integrated anti-fouling and anti-bacterial coating applications. European Polymer Journal 2022;170:111170. [DOI: 10.1016/j.eurpolymj.2022.111170] [Reference Citation Analysis]