Prostaglandins and congeners XXIII (1). Synthesis of 15-deoxy-16-hydroxy-16-methylprostaglandins. The importance of the C13-C14 trans double bond for bronchodilator activity
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference21 articles.
1. For paper XXII of this series, see M. B. Floyd, R. E. Schaub, G. J. Siuta, J. S. Skotnicki, C. V. Grudzinskas, M. J. Weiss, F. Dessy and L. VanHumbeeck, submitted for publication.
2. Synthesis and gastric antisecretory properties of 15-deoxy-16-hydroxyprostaglandin E analogs
3. Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives
4. Prostaglandins. X. Synthesis of prostaglandin models and prostaglandins by conjugage addition of a functionalized organocopper reagent
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1. An efficient synthesis of the antisecretory prostaglandin enisoprost;The Journal of Organic Chemistry;1991-03
2. Prostaglandins and congeners. 29. (16RS)-(.+-.)-15-Deoxy-16-hydroxy-16-vinylprostaglandin E2, an orally and transdermally active hypotensive agent of prolonged duration;Journal of Medicinal Chemistry;1982-05
3. Azaprostanoids I. Synthesis of (RAC)-8-aza-11-deoxy-15-deoxy-16-hydroxy-16-methylprostaglandins;Tetrahedron Letters;1982-01
4. Prostaglandins and congeners. 27. Synthesis of biologically active 16-halomethyl derivatives of 15-deoxy-16-hydroxyprostaglandin E2;The Journal of Organic Chemistry;1980-06
5. HMPA-Mediated conjugate addition of alkyl- and phenylthioallyl anions to cyclopentenone;Tetrahedron Letters;1980-01
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