Site-selective Suzuki cross-coupling reactions of 2,3-dibromobenzofuran |
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| Authors: | Nguyen Thai Hung Imran Malik Peter Langer |
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| Affiliation: | a Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany
b Leibniz-Institut für Katalyse e. V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany |
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| Abstract: | The Suzuki-Miyaura reaction of 2,3-dibromobenzofuran with two equivalents of boronic acids gave 2,3-diarylbenzofurans. The reaction with one equivalent of arylboronic acids resulted in site-selective formation of 2-aryl-3-bromobenzofurans. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from 2,3-dibromobenzofuran in a one-pot protocol by sequential addition of two different boronic acids. |
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| Keywords: | Catalysis Palladium Suzuki-Miyaura reaction Site-selectivity Benzofuran |
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