Abstract
AbstractAn efficient synthesis of paullone and kenpaullone derivatives in moderate to high yields has been achieved through photocyclizations of (2‐chloro‐1H‐indole‐3‐yl)‐N‐arylacetamides in acetone at room temperature. Paullone and kenpaullone have been obtained easily and in high yields by deprotection of the photocyclization products.
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