𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Enzymes of platelet activating factor synthesis in brain

✍ Scribed by R. Roy Baker

Publisher
Springer
Year
1995
Tongue
English
Weight
772 KB
Volume
20
Category
Article
ISSN
0364-3190

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Synthesis of heterocyclic platelet activ
Synthesis of heterocyclic platelet activating factor analogues
✍ JΓΌrgen Zeidler; Werner Zimmermann πŸ“‚ Article πŸ“… 1994 πŸ› Elsevier Science 🌐 English βš– 701 KB

The synthesis of heterocyclic analogues of the platelet activating factor is described. The preparation starts with acylating rac-tetrahydro-l,3-thiazine-4-carboxylic acid ethyl ester, with palmitoyl chloride to form the amide linkage. Following ester reduction, the phosphocholine part is introduced

Synthesis of heterocyclic platelet activ
Synthesis of heterocyclic platelet activating factor analogues
✍ JΓΌrgen Zeidler; Werner Zimmermann πŸ“‚ Article πŸ“… 1995 πŸ› Elsevier Science 🌐 English βš– 681 KB

The synthesis of heterocyclic analogues of the platelet activating factor is described. The preparation starts with acylating rac-tetrahydro-1,3-thiazine-4-carboxylic acid ethyl ester, with palmitoyl chloride to form the amide linkage. Following ester reduction, the phosphocholine part is introduced

Synthesis of azathia analogues of platel
Synthesis of azathia analogues of platelet activating factor with polyheterosidechains
✍ J.M. Zeidler; W. Zimmermann; H.J. Roth πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 English βš– 417 KB

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