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Reactions of 1-[2-(methylchalcogeno)phenyl]propenones with electrophiles gave α-(α-hydroxyalkyl)enones (Morita-Baylis-Hillman adducts) after the work-up of the reaction mixture with Et_3N. Electrophiles not only aldehydes but also α-diketones and α-keto esters were reactive to the reactions. Tricyclic compounds with a bridgehead bound to four heteroatoms were obtained from the reactions of 3-cinnamoyl-1,3-oxazolidine-2-thiones with aldehydes. Four stereocenters were simultaneously formed when an optically active thione was used. Tricyclic products were led to 1,3-diols bearing three consecutive stereocenters using acid hydrolysis, S-methylation and reductive removal of the chiral 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