Addition of 1-trimethylsilyloxybuta-1, 3-diene 2 to the quinones 4, 5, 6, 17, 18, 19, 20 bearing formyl, acetyl, methoxycarbonyl or carboxamide substituents at C-2, afforded the Diels-Alder adducts 11, 12, 13, 25, 26, 27, 28 whereas addition of 2-trimethylsilyloxyfuran 3 afforded the fragmentation products 29, 30, 31, 35, 36, 37, 38. Quinones 7, 21 bearing a carboxyl group at C-2 afforded 1, 4-naphthoquinone and 9, 10-anthracenedione with 2 and no adducts ...