Synfacts 2006(5): 0423-0423  
DOI: 10.1055/s-2006-934437
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 16S-Iloprost

Contributor(s): Philip Kocienski
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).