𝔖 Bobbio Scriptorium
✦   LIBER   ✦

STEREOSPECIFIC TOTAL SYNTHESIS OF CORTISONE

✍ Scribed by Sarett, L. H.; Arth, G. E.; Lukes, R. M.; Beyler, R. E.; Poos, G. I.; Johns, W. F.; Constantin, J. M.


Book ID
120620768
Publisher
American Chemical Society
Year
1952
Tongue
English
Weight
369 KB
Volume
74
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


THE TOTAL SYNTHESIS OF CORTISONE
✍ Woodward, R. B.; Sondheimer, Franz; Taub, David πŸ“‚ Article πŸ“… 1951 πŸ› American Chemical Society 🌐 English βš– 144 KB
Stereospecific total synthesis of cycloe
✍ Edward Y. Chen πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 226 KB

A stereospecific sequence from the allylic alcohol 3 to the new anti-biotic, cycloeudesmol 2, in 9 steps (21.7% overall yield) is described.

Stereospecific total synthesis of (.+-.)
✍ Corey, E. J.; Wess, Guenther; Xiang, Yi Bin; Singh, Ashok K. πŸ“‚ Article πŸ“… 1987 πŸ› American Chemical Society 🌐 English βš– 242 KB
CANTHARIDIN. A STEREOSPECIFIC TOTAL SYNT
✍ Stork, Gilbert; Tamelen, Eugene E. VAN; Friedman, Leonard J.; Burgstahler, Alber πŸ“‚ Article πŸ“… 1951 πŸ› American Chemical Society 🌐 English βš– 115 KB
Stereospecific total synthesis of ajugar
✍ Andrew S. Kende; Bruce Roth; Isao Kubo πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 259 KB

A stereospecific sequence from the octalindlone 2 leads In 21 steps to the new lnsecttcrde ajuqarin-IV. Formation of the butenohde portion is conveniently achteved from acid 21 by successive use of the reaqents trts(tr~methylsiloxy)ethylene and ketenyhdenetrtphenyl-phosphorane.