Prostaglandins and congeners VIII. An improved procedure for the conjugate addition of 3-oxy-E-1-alkenyl ligands via lithium alanate reagents. 11-deoxyprostaglandin E1 analogues
- 31 December 1975
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 16 (10) , 765-768
- https://doi.org/10.1016/s0040-4039(00)71978-2
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Synthesis of prostaglandins by alanate additions to cyclopentenones (1)Prostaglandins, 1973
- Prostaglandins and congeners I. The synthesis of 11,15-bisdeoxyprostaglandins E1, E2, and F1α. The stereospecific conjugate addition of a lithiumTetrahedron Letters, 1972
- Prostaglandins. X. Synthesis of prostaglandin models and prostaglandins by conjugage addition of a functionalized organocopper reagentJournal of the American Chemical Society, 1972
- Mixed cuprate reagents of type R1R2CuLi which allow selective group transferJournal of the American Chemical Society, 1972
- Prostaglandins. IV. Total syntheses of dl-11-deoxy PGE1 and 13,14-dihydro derivatives of 11-deoxy PGE1, PGF1.alpha. and PGF1.beta.The Journal of Organic Chemistry, 1972
- Studies on Polynucleotides. XIV.1 Specific Synthesis of the C3″-C5″ Interribonucleotide Linkage. Syntheses of Uridylyl-(3″→5″)-Uridine and Uridylyl-(3″→5″)-Adenosine2Journal of the American Chemical Society, 1962