Synthesis of 7-hydroxydibenzopyran-6-ones via benzannulation of coumarins

We have successfully demonstrated a facile synthesis of a variety of 7-hydroxydibenzopyran-6-ones via a two-step protocol from 3-acylcoumarins having a latent Nazarov dienone functionality. Condensation of 3-acylcoumarins and ethyl cyanoacetate under basic (wet K 2 CO 3 ) and microwave irradiation conditions followed by decarboethoxylative aromatization with Br 2 or DDQ furnished dibenzopyran-6-ones in high yields. The formation of ring C of the dibenzopyran-6-one motif critically depended on an active methylene compound and C7 substitution on coumarins. The Ar–Br or ArOTf substitution in dibenzopyran-6-ones was leveraged for the palladium-catalysed Suzuki coupling with diverse aryl boronic acids to increase the structural diversity. Reductive decyanation of C10 cyano dibenzopyran-6-ones furnished some of the isomers of urolithin A.