A highly efficient route to a key intermediate for the synthesis of A prostaglandins
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (2) , 107-109
- https://doi.org/10.1016/s0040-4039(01)84252-0
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- 1,4-Addition of the methylenecarbonyl unit (-CH2CO-) to dienesJournal of the American Chemical Society, 1971
- New reagents for stereoselective carbonyl reduction. Improved synthetic route to the primary prostaglandinsJournal of the American Chemical Society, 1971
- Stereospecific total synthesis of prostaglandins E3 and F3.alpha.Journal of the American Chemical Society, 1971
- Total synthesis of prostaglandins F1.alpha., E1, F2.alpha., and E2 (natural forms) from a common synthetic intermediateJournal of the American Chemical Society, 1970
- A new total synthesis of prostaglandins of the E1 and F1 series including 11-epiprostaglandinsJournal of the American Chemical Society, 1968
- Dipyridine-chromium(VI) oxide oxidation of alcohols in dichloromethaneTetrahedron Letters, 1968
- 507. A stereoselective synthesis of squaleneJournal of the Chemical Society, 1959