立体中心
对称化
对映选择合成
化学
咪唑
亲核细胞
双环分子
有机催化
硝基醛反应
硫脲
催化作用
有机化学
组合化学
立体化学
作者
Chenglong Hu,Xuyang Tang,Baochi Zhang,Zhenfeng Zhang,Wei‐Ping Deng,Wanbin Zhang
标识
DOI:10.1021/acscatal.3c05005
摘要
Thiourea-assisted chiral bicyclic imidazole organocatalysts were designed, synthesized, and successfully applied in the asymmetric acylative desymmetrization of P-prochiral bisphenols. Under mild conditions, the P-stereogenic products were obtained in high yields (up to 99% yield) and with high enantioselectivities (up to 99% ee). Most importantly, the reaction could also achieve satisfactory results under 1 mol % catalyst loadings. Mechanistic studies showed that the synergistic effect including the covalent activation of the acyl group by the nucleophilic imidazole and the noncovalent H-bonding and π-interaction between the catalyst and substrate was crucial for the efficient construction of P-stereocenters.
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