The paper describes the Suzuki cross-coupling of a variety of N and C-3 substituted 5-bromoindazoles with N-Boc-2-pyrrole and 2-thiopheneboronic acids. The reactions, performed in the presence of K2CO3, dimethoxyethane and Pd(dppf)Cl2 as catalyst, gave the corresponding adducts in good yields. The methodology allows the facile production of indazole-based heteroaryl compounds, a unique architectural motif that is ubiquitous in biologically active molecules. (This article belongs to the Section Organic Synthesis)

Migliorini, A., Oliviero, C., Gasperi, T., Loreto, M.A. (2012). The Suzuki Reaction Applied to the Synthesis of Novel Pyrrolyl and Thiophenyl Indazoles. MOLECULES, 17(4), 4508-4521 [10.3390/molecules1704450810.3390/molecules17044508].

The Suzuki Reaction Applied to the Synthesis of Novel Pyrrolyl and Thiophenyl Indazoles

GASPERI, TECLA;
2012-01-01

Abstract

The paper describes the Suzuki cross-coupling of a variety of N and C-3 substituted 5-bromoindazoles with N-Boc-2-pyrrole and 2-thiopheneboronic acids. The reactions, performed in the presence of K2CO3, dimethoxyethane and Pd(dppf)Cl2 as catalyst, gave the corresponding adducts in good yields. The methodology allows the facile production of indazole-based heteroaryl compounds, a unique architectural motif that is ubiquitous in biologically active molecules. (This article belongs to the Section Organic Synthesis)
2012
Migliorini, A., Oliviero, C., Gasperi, T., Loreto, M.A. (2012). The Suzuki Reaction Applied to the Synthesis of Novel Pyrrolyl and Thiophenyl Indazoles. MOLECULES, 17(4), 4508-4521 [10.3390/molecules1704450810.3390/molecules17044508].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11590/116356
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