Fremgangsmåde til fremstilling af diastereomerrene 4-acetoxy-3-hydroxyethyl-azetidinoner
4-Acetoxy-3-hydroxyethylazetidinone of the formula in particular 4(R)-acetoxy-3(R)-(1'(R)-hydroxyethyl)-2-azetidinone, is prepared from enantiomerically pure compounds of the formula in which R denotes lower alkyl and Z denotes amino, arylmethylamino, acylamino or azido, by reduction of the C=C...
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Zusammenfassung: | 4-Acetoxy-3-hydroxyethylazetidinone of the formula in particular 4(R)-acetoxy-3(R)-(1'(R)-hydroxyethyl)-2-azetidinone, is prepared from enantiomerically pure compounds of the formula in which R denotes lower alkyl and Z denotes amino, arylmethylamino, acylamino or azido, by reduction of the C=C double bond and optionally of the arylmethylamino or azido group with hydrogen, lactone ring opening, ring closure to the beta -lactam, if appropriate after hydrolysis of the acylamino group, and oxidative decarboxylation of the original lactone carboxyl group in the presence of an acetate-releasing agent. Compounds of the formula I can be used as starting substances for the preparation of beta -lactam antibiotics. Novel intermediates and starting materials are also described. |
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