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Palladium-Catalyzed Decarboxylative Benzylation of β-Keto Esters

机译:钯催化β-酮酯的脱羧苄基化

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Palladium-catalyzed decarboxylative allylation of allylic β-ketocarboxylates, which was originally developed by Tsuji and Saegusa, has intensively been studied recently, including asymmetric variants. The decarboxylative allylation was involved With (π-allyl)palladium intermediate. Meanwhile, we have developed palladium-catalyzed nucleophilic substitutions of benzylic carbonates recently. As with Tsuji-Trost reaction, the benzylic carbonate reacts with palladium(0) to give (π-benzyl)palladium, which readily undergoes nucleophilic attack. In this context, we resolved to engage in the actualization of the palladium-catalyzed decarboxylative benzylation of benzyl β-ketocarboxylates.
机译:最近研究最初由Tsuji和Saegusa开发的烯丙基β-酮羧酸酯的钯催化的烯醇羧酸烯醇化烯丙基化,包括不对称变体。脱羧烯化与(π-烯丙基)钯中间体涉及。同时,我们最近开发出钯催化的苄基碳酸核酸核酸核酸酯。与Tsuji-trost反应一样,苄基碳酸酯与钯(0)反应,得到(苄基)钯,其容易经历亲核发作。在这种情况下,我们决定从事苄基β-酮羧酸盐的钯催化的脱羧苄基化。

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