Abstract

Palladium-catalyzed Heck reaction of oreoselone trifluoromethanesulfonate with various terminal alkenes (methyl acrylate, styrene, vinylpyridines, N-vinylpyrrole, and N-vinyl-1,2,4-triazole) led to the formation of the corresponding (E)-3-vinyl-7H-furo[3,2-g]chromen-7-ones. The yield was found to depend on the catalytic system and initial olefin structure.

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