Synthesis of 2-Oxazolones and α-Aminoketones via Palladium-Catalyzed Reaction of β,β-Dibromoenamides
β,β-Dibromoenamides show two different interesting reactivities based on the choice of R group under the reaction conditions. On the basis of mechanistic studies, both reactions proceed via an intermolecular Suzuki−Miyaura C−C coupling and an intramolecular C−O coupling.
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Veröffentlicht in: | Organic letters 2011-01, Vol.13 (1), p.106-109 |
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container_title | Organic letters |
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creator | Chai, David I Hoffmeister, Laura Lautens, Mark |
description | β,β-Dibromoenamides show two different interesting reactivities based on the choice of R group under the reaction conditions. On the basis of mechanistic studies, both reactions proceed via an intermolecular Suzuki−Miyaura C−C coupling and an intramolecular C−O coupling. |
doi_str_mv | 10.1021/ol102634c |
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title | Synthesis of 2-Oxazolones and α-Aminoketones via Palladium-Catalyzed Reaction of β,β-Dibromoenamides |
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