化学
薗头偶联反应
芳基
钯
催化作用
有机化学
羰基化
一氧化碳
烷基
作者
Yanhua Zhao,Xing‐Wei Gu,Xiao‐Feng Wu
标识
DOI:10.1021/acs.orglett.4c03519
摘要
Herein, we developed a mild and efficient palladium-catalyzed carbonylative Sonogashira coupling of aryl thianthrenium salts with aliphatic alkynes and benzyl acetylene toward alkynones and furanones. Various desired products were prepared in good yields with broad functional group tolerance including the bromide group. In the case of using benzyl acetylene, the corresponding furanones can be obtained in good yields under the same conditions with two molecules of CO inserted.
科研通智能强力驱动
Strongly Powered by AbleSci AI