Synthesis, Inhaltsverzeichnis Synthesis 2015; 47(23): 3767-3775DOI: 10.1055/s-0035-1560456 paper © Georg Thieme Verlag Stuttgart · New YorkSynthesis of Heteroaryl ortho-Phenoxyethylamines via Suzuki Cross-Coupling: Easy Access to New Potential Scaffolds in Medicinal Chemistry Autor*innen Institutsangaben Leda Ivanova Manasieva Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy eMail: silvia.franchini@unimore.it Battisti Umberto Maria Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy eMail: silvia.franchini@unimore.it Adolfo Prandi Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy eMail: silvia.franchini@unimore.it Livio Brasili Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy eMail: silvia.franchini@unimore.it Silvia Franchini* Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy eMail: silvia.franchini@unimore.it Artikel empfehlen Abstract Artikel einzeln kaufen(opens in new window) Alle Artikel dieser Rubrik(opens in new window) Abstract Heteroaryl ortho-phenoxyethylamines have been extensively employed in medicinal chemistry as privileged scaffolds for the design of highly potent and selective ligands. Herein an efficient, fast, and general method for the synthesis of heteroaryl phenoxyethylamines via Suzuki cross-coupling is reported. This approach offers the opportunity to obtain a large variety of biaryls incorporating five-membered (thiophene, furan, thiazole, pyrazole, imidazole) or six-membered (pyridine, pyrimidine) heteroaromatic rings for appropriate libraries of ligands. All the compounds presented here have never been synthesized before and a full structural characterization is given. Key words Key wordsC–C coupling - heterocycles - palladium - Suzuki–Miyaura cross-coupling - building blocks Volltext Referenzen References 1 Walter MW, Hoffman BJ, Gordon K, Johnson K, Love P, Jones M, Man T, Phebus L, Reel JK, Rudyk HC, Shannon H, Svensson K, Yu H, Valli MJ, Porter WJ. Bioorg. Med. Chem. 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