Intramolecular sulfenyl bromide addition promising a new synthetic route to 9(O)-thiaprostacyclin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregation
2. Arterial walls are protected against deposition of platelet thrombi by a substance (prostaglandin X) which they make from prostaglandin endoperoxides
3. The chemical structure of prostaglandin X (prostacyclin)
4. Prostacyclin (PGX) is the endogeneous metabolite responsible for relaxation of coronary arteries induced by arachidonic acid
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3. Enethiolizable Thioacylsilanes as Intermediates for the Synthesis of Thietanols, Thiolanols, and Thianols;European Journal of Organic Chemistry;2000-07
4. Synthesis of cyclic sulfides by intramolecular ring opening of epoxides by thiolates generated by nickel complex catalyzed electroreduction of thioacetates;Tetrahedron Letters;2000-04
5. Synthesis of cyclic sulfides by nickel complexes catalyzed electroreduction of unsaturated thioacetates and thiosulfonates;Tetrahedron Letters;1998-10
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