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.
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