羧化
化学
固碳
双功能
催化作用
基质(水族馆)
烷基
组合化学
有机催化
卤化物
有机化学
二氧化碳
对映选择合成
海洋学
地质学
作者
Junbin Shi,Qingqing Bu,Binyuan Liu,Bin Dai,Ning Liu
标识
DOI:10.1021/acs.joc.0c02673
摘要
An organocatalytic strategy for the direct carboxylation of terminal alkynes with CO2 has been developed. The combined use of a bifunctional organocatalyst and Cs2CO3 resulted in a robust catalytic system for the preparation of a range of propiolic acid derivatives in high yields with broad substrate scope using CO2 at atmospheric pressure under mild temperatures (60 °C). This work has demonstrated that this organocatalytic method offers a competitive alternative to metal catalysis for the carboxylation of terminal alkynes and CO2. In addition, this protocol was suitable for the three-component carboxylation of terminal alkynes, alkyl halides, and CO2.
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