Recent Advances on the Role of Cu-Nanoparticles in the Organic Transformations
Abstract
Copper nanoparticles explored the most useful class of heterogeneous catalyst in various chemical transformations. Copper nanoparticles has attracted much more attention because of its promising activity, high atom economy, better yield, shorter reaction times, inexpensive, recyclability, low catalyst loading. These approaches open new possibilities in, click reactions, C-N and C-S cross coupling reaction, fixation of CO2, KA3 and A3 coupling, aziridine ring opening reactions. This review covers some useful organic transformations which were carried out in presence of various copper-nanoparticles.
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Chatterjee R, Santra S, Ghosal NC, Giri K, Zyryanov GV, Majee A, Chemistry Select. 2020, 5, 4525–4529.
Kolb HC, Finn MG, Sharpless, KB, Chem. Int. Ed. 2001, 40, 2004−2021.
Huisgen R, Knorr R, Mö bius L, Szeimies G. Chem. Ber. 1965, 98, 4014−402.
Bock VD, Hiemstra H, Van Maarseveen J. Eur. J. Org. Chem. 2006, 51–68
Alonso F, Moglie Y, Radivoy G, Yus M, Adv. Synth. Catal. 2010, 352, 3208−3214.
Alinezhad H, Pakzad K. Organometal Chem. 2019, 5144.
Dhrubajyoti A, Das TG, Suman Thakura, Karaka NJ, Thakur A. Catalysis Communication. 2015, 59, 238–243.
Khatuna R, Biswasa S, Biswasa IH, Riyajuddinb S, Haquea N, Ghoshb K, Isla SM. Elsevier Ltd. 2020, 40, 2212–9820.
Modak A, Nett AJ, Swift EC, Haibach MC, Chan VS, Franczyk TS, Shekhar S, Cook SP. ACS Catal. 2020, 10, 10495–10499.
Reddy PL, Arundhathi R, Tripathia M, Rawat, DS. RSC Adv. 2016, 6, 53596–53601.
Dutta A, Chetia M, Ali AA, Bordoloi A, Gehlot PS, Kumar A, Sarma D, Catalysis Letters. 2016, 149, (1), 141–150.
Tojo Gabriel, Fernandez IM. Springer, 2006.
Rawat M, Rawat DS. ACS 2020, 8, (36), 13701–13712.
Albaladejo MJ, Alonso F, González-Soria MJ. ACS Catal. 2015, 5, 3446–3456
BS, V Vasava P. Elsevier. 2019, (21), 100416.
Shah J, Jan MR. 2014, 109, 196–204.
Peshkov VA, Pereshivko OP, Eycken, EVV. Chem. Soc. Rev. 2012, 10, 3790–3807.
Saha TK, Das R, Chemistry Select 2018, 3 147–169.
Nandishaiah R, Panduga V, Reddy J, K. Sambandamurthy V, Sriram D, ACS Med. Chem. Lett. 2014, 5, 820–825.
Sreedhar B, Arundhathi R, Reddy PL, Kantam ML. J. Org Chem 2009, 74, 7951–7954.
Reddy PL, Arundhathi R, Tripathia M, Rawat DS. RSC Adv 2016, 6, 53596–53601.
Nandi D, Perla VK. Nature 2020, 10, 16720.
Kolb Finn HC, Sharpless MG, Chemistry KBC. Angew. Chem. Int. 2001, 40.
Xi WX, Scott TF, Kloxin CJBNC. Adv. Funct. Mater 2014, 24, 2572–2590.
Fong Andrews DA, GA. Polym. Chem 2018, 9, 2873–2879.
Erfan MA, Akhlaghinia DB, Ghodsinia SSE. Chem Select. 2020, 5, 2306–2316.
Alonso F, Moglie Y, Radivoy G, Acc Chem. Res. 2015, 48, 2516.
Raiza AJ, Pandian PK, Kumar RG. Chem Select. 2019, 4, (6), 1964–1970.
Gea X, Gea M, Chenb X, Qianb C, Liua X, Zhoub S. Mol. Catal. 2020, 484, 110726.
Sayahi MH, Bahadorikhalili S, Saghanezhad SJ, Mahdavi M, Res Chem Intermed. 2018, 44, 5241–5253.
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