合成子
对映选择合成
化学
催化作用
手性路易斯酸
原子经济
路易斯酸催化
氢原子
铑
组合化学
光催化
路易斯酸
有机化学
烷基
作者
Yulong Kuang,Kai Wang,Xiangcheng Shi,Xiaoqiang Huang,Eric Meggers,Jie Wu
标识
DOI:10.1002/anie.201910414
摘要
Abstract Enantioenriched 1,4‐dicarbonyl compounds are versatile synthons in natural product and pharmaceutical drug synthesis. We herein report a mild pathway for the efficient enantioselective synthesis of these compounds directly from aldehydes through synergistic cooperation between a neutral eosin Y hydrogen atom transfer photocatalyst and a chiral rhodium Lewis acid catalyst. This method is distinguished by its operational simplicity, abundant feedstocks, atom economy, and ability to generate products in high yields (up to 99 %) and high enantioselectivity (up to 99 % ee ).
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