𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A general methodology for pseudoguaiane synthesis: total synthesis of (.+-.)-damsinic acid and (.+-.)-confertin

✍ Scribed by Wender, Paul A.; Eissenstat, Michael A.; Filosa, Michael P.


Book ID
126871398
Publisher
American Chemical Society
Year
1979
Tongue
English
Weight
391 KB
Volume
101
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A facile entry to pseudoguaianes. Total
✍ Peter T. Lansbury; Algirdas K. Serelis πŸ“‚ Article πŸ“… 1978 πŸ› Elsevier Science 🌐 French βš– 207 KB

Among the various classes of sesquiterpene a-methylene-y-butyrolactones, the pseudoguaianolides' are unparalleled as structural and stereochemical challenges2 to the discriminating synthetic organic chemist. I II III We herein report an extremely facile pseudoguaiane construction of potential value

A general methodology for the asymmetric
✍ Om V Singh; Hyunsoo Han πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 French βš– 314 KB

A general methodology for the stereoselective synthesis of 1-deoxymannojirimycin and its three other stereoisomers is described. The achiral olefin 6 was converted through the common olefin intermediate 12 to the target compounds in a highly stereocontrolled manner. The regioselective asymmetric ami