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Enantioselective Catalytic Allylation of Carbonyl Groups by Umpolung of -Allyl Palladium Complexes

机译:-烯丙基钯配合物的Uppolung对羰基的对映选择性催化烯丙基化

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摘要

The development of catalytic asymmetric C-C bond-forming reactions remains one of the main challenges in organic chemistry. Transformations mediated by transition-metal complexes with properly designed ligands have enabled this challenging synthetic goal to be achieved, often with remarkable results. Among the transition-metal-catalyzed reactions known to form C-C bonds, the palladium-catalyzed allylic substitution developed by Trost and Tsuji stands out as one of the most valuable synthetic tools available.
机译:催化不对称C-C键形成反应的发展仍然是有机化学中的主要挑战之一。由过渡金属配合物与适当设计的配体介导的转化,使这一具有挑战性的合成目标得以实现,通常具有显着结果。在已知形成C-C键的过渡金属催化的反应中,由Trost和Tsuji开发的钯催化的烯丙基取代是最有价值的合成工具之一。

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