Synthesis of Prostaglandins and their congeners I. (+)-11-deoxy-11α-hydroxymethyl prostaglandin F2α from aucubin
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (3), 251-254
- https://doi.org/10.1016/s0040-4039(01)85938-4
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Synthesis of (R)- and (S)-4-hydroxy-2-cyclopentenonesTetrahedron Letters, 1976
- Chiral synthesis of prostaglandins from carbohydrates. Synthesis of (+)-15-(S)-prostaglandin A2Journal of the American Chemical Society, 1976
- Prostaglandins. I. Direct synthesis of optically active Corey-intermediate from (S)-(-)-malic acidJournal of the American Chemical Society, 1976
- Prostaglandin chemistry—VTetrahedron, 1976
- Total syntheses of 11-deoxy-11α-hydroximethyl prostacrlandin EsTetrahedron Letters, 1975
- The synthesis of prostaglandin endoperoxide analogsTetrahedron Letters, 1975
- Preparation of an optically active prostaglandin intermediate via asymmetric inductionJournal of the American Chemical Society, 1975
- Versatile prostaglandin synthesis. Use of a carboxy-inversion reactionThe Journal of Organic Chemistry, 1973
- Total synthesis of prostaglandins. IV. Completely stereospecific synthesis of prostaglandin E1Journal of the American Chemical Society, 1973
- Stereochemistry of AucubinNippon kagaku zassi, 1964