𝔖 Bobbio Scriptorium
✦   LIBER   ✦

General methodology for cis-hydroisoquinoline synthesis: synthesis of reserpine

✍ Scribed by Wender, P. A.; Schaus, J. M.; White, A. W.


Book ID
126145580
Publisher
American Chemical Society
Year
1980
Tongue
English
Weight
398 KB
Volume
102
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Synthesis studies directed toward gelsem
✍ William G. Earley; E.Jon Jacobsen; G. Patrick Meier; Taeboem Oh; Larry E. Overma πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 399 KB

## Cis-Hydrowquinolmes can be prepared in good yields by treatment of read@ available endo-l-(cyanomet~l)~-~~o~bydroxyblcyclo[222Jocr-5-en-l -yl anunes wth KH as summan zed m Scheme 3 Gelsermne (1). the mayor alkaknd of g&emu&a sernpervirens (Carolina or yellow psrmne) was first

Diels–Alder reactions of phenylglycinol-
✍ NΓΊria Casamitjana; Mercedes Amat; NΓΊria Llor; MarΓ§al Carreras; Xavier Pujol; M. πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 English βš– 302 KB

The diastereomeric phenylglycinol-derived unsaturated d-lactams trans-3 and cis-3 react with dienes with exo facial diastereoselectivity to give the corresponding tricyclic adducts, which were ultimately converted to enantiomeric cis-hydroisoquinolines.

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