Synthesis and anti-ulcer activity of 16-phenoxy analogues of (+)-11-deoxyprostaglandin E1

Author:

Banerjee A.K.,Broughton B.J.,Burton T.S.,Caton M.P.L.,Christman A.J.,Coffee E.C.J.,Crowshaw K.,Hardy C.J.,Heazell M.A.,Palfreyman M.N.,Parker T.,Saunders L.C.,Stuttle K.A.J.

Publisher

Elsevier BV

Subject

Endocrinology,Biochemistry

Reference8 articles.

1. Synthesis and gastrointestinal pharmacology of some 15- and 16- modified (+)-11-deoxy-prostaglandins;Banerjee;Prostaglandins,1978

2. Synthesis and antifertility activity of ω-chain phenyl- and 16-phenoxy-analogues of (+)-11-deoxy-prostaglandin Fα;Broughton;Prostaglandins,1980

3. Die Fluorolyse metallorganischer bindungen durch perchloryl fluorid;Schlosser;Chem. Ber.,1969

4. Nucleophilic substitutions of α-halogenoketones. XVII. Nucleophilic substitutions and β-elimination in the acetolysis of 1 1-chloro-4-phenyl1-4-phenylthio-2-butanone;Rosnati;Gazz. Chem. Ital.,1976

5. Effects of anti-ulcer agents on indomethacin-induced gastric ulceration in the rat;Lee;Arch. Int. Pharmacodyn.,1971

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