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Synthesis of azathia analogues of platelet activating factor with polyheterosidechains

✍ Scribed by J.M. Zeidler; W. Zimmermann; H.J. Roth


Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
417 KB
Volume
55
Category
Article
ISSN
0009-3084

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✦ Synopsis


The synthesis of azathia analogues of the platelet activating factor with oxygen and sulphur-containing sidechains is reported. The starting point is 1-acetylthio-3-hydroxy-2-propaneamine-HCl, which permits the formation of the thioether and the acetamido linkage in one step. The phosphocholine part is introduced via 2-chloro-2-oxo-l,3,2-dioxaphospholane and subsequent ring opening with trimethylamine under pressure.


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