摘要
Photo-irradiation of 2-(5-methylthiophen-2-yl)-3-[(naphthalen-2-yl)methoxy]-4H-chromen-4-ones yielded the fascinating angular tetracyclic products via cyclization involving both 2-thienyl ring and naphthylmethoxy group via 1,4-biradical generated in the Norrish type-II process. The stereochemical dispositions of the products were determined by MM2 energy minimized programme and spectroscopic analysis.
Photo-irradiation of 2-(5-methylthiophen-2-yl)-3-[(naphthalen-2-yl)methoxy]-4H-chromen-4-ones yielded the fascinating angular tetracyclic products via cyclization involving both 2-thienyl ring and naphthylmethoxy group via 1,4-biradical generated in the Norrish type-II process. The stereochemical dispositions of the products were determined by MM2 energy minimized programme and spectroscopic analysis.