化学
烷基化
对映选择合成
催化作用
对映体
级联
组合化学
氯甲酸盐
分子
有机化学
色谱法
作者
Jian Chen,Gao Deng,You Wang,Shaolin Zhu
标识
DOI:10.1002/cjoc.202200491
摘要
Comprehensive Summary NiH‐catalyzed multicomponent reductive hydrofunctionalization of alkenes is an attractive but poorly explored approach to rapidly increasing molecular complexity. In this process, the selective generation of the desired product can be challenging. Herein, we report that a highly chemo‐, regio‐ and enantioselective reductive hydrocarbonylation of alkenes has been achieved using a chloroformate ester as a source of CO. A wide range of structurally diverse α‐hydroxy ketones, privileged structural elements in bioactive molecules and useful building blocks, were obtained from such reactions with high enantiomeric purity.
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