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ChemInform Abstract: SYNTH. NEUER BICYCLISCHER PROSTAGLANDINE DURCH PHOTOCYCLOADDITIONEN
Abstract: Durch Überführung des Hydroxyjodlactons (I) in das ungesättigte Lacton (II), alkalische Öffnung des Lactonringes, Veresterung der entstehenden Hydroxysäure (IIIa) und Chromsäureoxidation des Methylesters (IIIb) wird das Enon (IV) dargestellt.
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