Synthesis, Table of Contents Synthesis 2017; 49(03): 685-692DOI: 10.1055/s-0036-1588319 paper © Georg Thieme Verlag Stuttgart · New YorkNano-Magnetic Sulfonic Acid Catalyzed Facile Synthesis of Diverse Amide Derivatives Jagatheeswaran Kothandapani Department of Chemistry, School of Chemical and Biotechnology, SASTRA University, Thanjavur 613401, India Email: selva@biotech.sastra.edu , Asaithampi Ganesan Department of Chemistry, School of Chemical and Biotechnology, SASTRA University, Thanjavur 613401, India Email: selva@biotech.sastra.edu , Subramaniapillai Selva Ganesan* Department of Chemistry, School of Chemical and Biotechnology, SASTRA University, Thanjavur 613401, India Email: selva@biotech.sastra.edu› Author AffiliationsRecommend Article Abstract Buy Article All articles of this category Abstract The excellent surface catalytic potential of Fe3O4–OSO3H is utilized in the synthesis of symmetrically and unsymmetrically substituted urea derivatives via transamidation reactions. The scope of the surface catalysis is further extended in transamidation reactions of cyclic and acyclic amide derivatives, and in the amidation of fatty acids. In both transamidation and amidation reactions, the catalyst is reusable up to five times without significant loss in its activity. Key words Key wordsmagnetic sulfonic acid - green synthesis - transamidation - fatty acid amidation - chemoselectivity Full Text References References 1a Divito EB, Cascio M. Chem. Rev. 2013; 113: 7343 1b Kaufmann D, Bialer M, Shimshoni JA, Devor M, Yagen B. J. Med. Chem. 2009; 52: 7236 1c Ganesh T, Jiang J, Yang M.-S, Dingledine R. J. Med. Chem. 2014; 57: 4173 1d Zheng X, Bauer P, Baumeister T, Buckmelter AJ, Caligiuri M, Clodfelter KH, Han B, Ho Y.-C, Kley N, Lin J, Reynolds DJ, Sharma G, Smith CC, Wang Z, Dragovich PS, Gunzner-Toste J, Liederer BM, Ly J, O’Brien T, Oh A, Wang L, Wang W, Xiao Y, Zak M, Zhao G, Yuen PW, Bair KW. J. Med. 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