Synthesis of 5-Cinnamoyl-3,4-dihydropyrimidine-2(1H)-ones

<div><p></p><p>Two different approaches to the synthesis of 1-unsubstituted 5-cinnamoyl-3,4-dihydropyrimidine-2(1H)-ones have been developed. The first includes N(1)-protection of the starting 5-acetyl-3,4-dihydropyrimidine-2(1H)-one, further Claisen–Schmidt reaction, and cleavage of the protecting group. The second approach consists of one-pot condensation of urea, aldehyde, and cinnamoylacetone as dicarbonyl component. The 5-cinnamoylderivative synthesis starting from 5-acetyl-1,3-dialkyl-3,4-dihydropyrimidine-2(1H)-ones is also shown.</p> </div

Microstructurally controlled polymers of rac-lactide by lithium complexes

International audienceA series of polylactides was prepared by stereoselective ring-opening polymerization of rac-lactid