Abstract

AbstractAn 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 CO2 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.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.