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Photochemistry of 3-alkoxychromones: photocyclisation of 2-aryl-6-chloro-3-{(thiophen-2-yl)methoxy}chromones

1,4-Biradicals generated upon photo-irradiation of 2-aryl-3-{(thiophen-2-yl)methoxy}chromones produced angular tetracyclic products bearing the thienyl group. The dehydrogenation and ring contraction products were also observed depending upon the electron density on the 2-aryl ring.

alkoxychromone; type-II reaction; 1,4-biradical; ring contraction; angular tetracyclic


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