SYNTHESIS OF CHIRALS REGIOISOMERS FROM D-MANNITOL: OBTAINMENT OF A ACETYLENIC ALCOHOLS MIXTURE. The synthesis of chiral acetylenic regioisomers was described by using an appropriate intermediate such as isopropylidene glycerol, a synthon widely used in the enantioselective syntheses. This intermediate was prepared from D-mannitol. The nine obtained compounds have been characterized by their respective spectral data. The mixture of chiral acetylenic alcohols showed activity against Escherichia coli when tested through the monitoring of CO(2) released during microbial respiration by using a conductimetric system.32923552359