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Synthesis of new stable analogues of prostacyclin: (±)-6a-oxo-6,9-metrano-15-hydroxyprosta-5,13-dienoic acids

✍ Scribed by C.W. Bird; H.I. Butler; M.P.L. Caton; E.C.J. Coffee; C.J. Hardy; T.W. Hart; H.J. Mason


Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
203 KB
Volume
26
Category
Article
ISSN
0040-4039

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✦ Synopsis


The synthesis is described of (fi)-6a-oxo-6,9-methano-L5-hydroxyprosta-5,13-dienoic acids as stable analogues of prostacyclin with blood platelet aggregation inhibiting activity. Considerable effort has been devoted to the preparation of chemically stable analogues prostacyclin.' We report here the synthesis of a new class of biologically active of analogues in which the 6,9 ether linkage of 11-deoxyprostacyclin is replaced by a carbonyl group to give the stable enone (15). -Scheme1


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