立体中心
对映选择合成
化学
亲核细胞
配体(生物化学)
组合化学
钯
烯丙基重排
催化作用
手性配体
筑地反应
阳离子聚合
对称化
立体化学
有机化学
受体
生物化学
作者
Kohsuke Ohmatsu,Takashi Ooi
标识
DOI:10.5059/yukigoseikyokaishi.73.140
摘要
A new strategy for the design of a chiral ligand for asymmetric transition-metal catalysis has been developed. Our strategy is based on the development of achiral cationic ammonium-phosphine hybrid ligands paired with readily available chiral anions. These ion-paired chiral ligands impart a remarkable stereocontrolling ability to their palladium complexes, which catalyze highly enantioselective allylic alkylations of prochiral carbon nucleophiles. Moreover, the exploitation of ion-paired chiral ligands in combinatorial screening has enabled the rapid identification of the optimal ligand for the palladium-catalyzed new asymmetric allylation reaction. We also developed a highly enantio- and diastereoselective [3+2] annulation reaction of 5-vinyloxazolidinones and activated trisubstituted alkenes catalyzed by a palladium complex bearing a different type of ion-paired ligand, which allows for the single-step construction of three contiguous stereocenters, including vicinal all-carbon quaternary stereocenters.
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