化学
铑
吲唑
酒
芳基
立体选择性
药物化学
烯丙基重排
碳酸盐
催化作用
立体化学
烯丙醇
有机化学
组合化学
烷基
作者
Xiang Zhao,Junwei Huang,Yadong Feng,Xiuling Cui
标识
DOI:10.1002/ejoc.202300823
摘要
Abstract An efficient rhodium(III)‐catalysed C−H activation of 3‐aryl‐1‐ H ‐indazoles with easily available vinylethylene carbonate has been reported. A series of allyl alcohol substituted 3‐aryl‐1‐ H ‐indazoles were obtained with broad functional groups tolerance and favourable stereoselectivity. Notably, C−H and C−O bonds were selectively activated in “one pot” manner, releasing CO 2 as the sole by‐product and avoiding external oxidant. This protocol provides a powerful approach for the post stage C−H allylation of indazole‐based substrates.
科研通智能强力驱动
Strongly Powered by AbleSci AI