Stereochemical course of the modified polonovski reaction and mercuric acetate oxidation in the preparation of 2-substituted 1,2,3,4,6,7,12,12b-octahydroindolo[2, 3-a]quinolizines
β Scribed by Mauri Lounasmaa; Esko Karvinen
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 543 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Application of the Mercuric Acetate-Edetic Acid Oxidation Method to the Synthesis of 2,3,4,5,6,7, quinolizines. -Application of the oxidation method to the substituted azaindoles (I), (III), and (V) results in direct formation of the azaindoloquinolizidine only in the case of (I). Educts (III) and
## Stereochemical control ' the preparation of 2substituted 1,2,3,4,6,7,12,12b-octahy~~oindoloI2,3-a,quinolizines possessing at will the C(12b)H-C(2)H cis or configuration trans was achieved by catalytic reduction ofthe 2,3-dehydro analoques, which were either unsubstituted on the indole nitrogen