Unexpected palladium catalyzed O-arylation occurring in 4-(4-fluoro-3-nitrophenyl)-1,2-dimethyl-5-nitro-1H-imidazole series
Autor: | Kevin Neilde, Laura Zink, Maxime D. Crozet, Patrice Vanelle |
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Přispěvatelé: | Chimie, biologie et radicaux libres - UMR 6517 (CBRL), Université de la Méditerranée - Aix-Marseille 2-Université Paul Cézanne - Aix-Marseille 3-Université de Provence - Aix-Marseille 1-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie Radicalaire (ICR), Aix Marseille Université (AMU)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) |
Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
inorganic chemicals
Reaction conditions Nitroimidazole 010405 organic chemistry Organic Chemistry chemistry.chemical_element 010402 general chemistry 01 natural sciences Biochemistry Medicinal chemistry 0104 chemical sciences Catalysis chemistry.chemical_compound chemistry Drug Discovery Nitro Imidazole [CHIM]Chemical Sciences Palladium |
Zdroj: | Tetrahedron Letters Tetrahedron Letters, Elsevier, 2012, 53 (40), pp.5393--5397. ⟨10.1016/j.tetlet.2012.07.107⟩ Tetrahedron Letters, 2012, 53 (40), pp.5393--5397. ⟨10.1016/j.tetlet.2012.07.107⟩ |
ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2012.07.107⟩ |
Popis: | International audience; We describe herein a new unexpected palladium-catalyzed O-arylation reaction in fluorinated nitro(o-nitrophenyl)imidazole series involving arylboronic acids under Suzuki-Miyaura cross-coupling reaction conditions. (C) 2012 Elsevier Ltd. All rights reserved. |
Databáze: | OpenAIRE |
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