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Synfacts 2006(5): 0423-0423
DOI: 10.1055/s-2006-934437
DOI: 10.1055/s-2006-934437
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York
Synthesis of 16S-Iloprost
G. J. Kramp, M. Kim, H.-J. Gais*, C. Vermeeren
RWTH Aachen, Germany
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Publikationsverlauf
Publikationsdatum:
21. April 2006 (online)
Significance
Iloprost is used for the treatment of arterial occlusion and pulmonary arterial hypertension. It is produced as a 1:1 mixture of 16S and 16R diastereoisomers but the 16S diastereoisomer is 20 times more active than the 16R analogue. The present synthesis is the first fully stereoselective synthesis of the more potent 16S isomer. Noteworthy steps include the asymmetric desymmetrization of the meso-ketone A, the conjugate addition of the alkenylcopper reagent to azoalkene B and the asymmetric Horner-Wadsworth-Emmons reaction to secure the E-trisubstituted alkene (D to E).