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Palladium-Catalyzed Decarbonylative Dehydration for the Synthesis of α-Vinyl Carbonyl Compounds and Total Synthesis of (−)-Aspewentins A, B, and C

机译:钯 - 催化脱氧羰基化脱水用于合成α-乙烯基羰基化合物和( - ) - Aspewentins A,B和C的总合成

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摘要

The direct α-vinylation of carbonyl compounds to form a quaternary stereocenter is a challenging transformation. It was discovered that δ-oxocarboxylic acids can serve as masked vinyl compounds and be unveiled by palladium-catalyzed decarbonylative dehydration. The carboxylic acids are readily available through enantioselective acrylate addition or asymmetric allylic alkylation. A variety of α-vinyl quaternary carbonyl compounds are obtained in good yields, and an application in the first enantioselective total synthesis of (−)-aspewentins A, B, and C is demonstrated.
机译:羰基化合物的直接α-乙烯基化以形成季立体中心是一项具有挑战性的转变。已经发现,δ-氧代羧酸可以用作掩蔽的乙烯基化合物,并通过钯催化的脱羰基脱水作用而公开。通过对映选择性丙烯酸酯加成或不对称烯丙基烷基化可容易地获得羧酸。以高收率获得了多种α-乙烯基季羰基化合物,并且证明了其在(-)-半萜烯A,B和C的第一对映选择性全合成中的应用。

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