SYNTHESIS OF OPTICALLY PURE 4-ARYL-2-HYDROXYTHETRONIC ACIDS.

摘要

THE PRESENT INVENTION REFERS TO A METHOD FOR SYNTHESIS OF 4-ARIL-2-HYDROXYTHETRONIC ACIDS, STEREOGENICALLY OPTICALLY PURE LABILS OF AN OPTICALLY PURE ALDEHYDE. THE INVENTION FURTHER REFERS TO THE USE OF SUCH OPTICALLY PURE COMPOUNDS AS POWERFUL INHIBITORS OF PLATE AGGREGATION WORKING AT THE LEVEL OF CYCLLOXYGENASE, AND ADDITIONALLY AS CYCLLOXYGENASE AND 5-LIPOXIGE INHIBITORS. THE INVENTION FURTHER REFERS TO THE PHARMACEUTICAL USE OF SUCH COMPOUNDS IN THE TREATMENT OF CORONARY ARTERIAL DISEASES, ESPECIALLY IN THE TREATMENT AND / OR PREVENTION OF ATEROSCLEROSIS, AND IN THE TREATMENT OF DIFFERENT INFLAMMATORY PATHOLOGIES, ESPECIALLY ARTRITIS.