The first synthesis of optically pure biscarbazoles and determination of their absolute configurations
β Scribed by Guoqiang Lin; Aimin Zhang
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 242 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Optically pure dimeric O-demethylmurrayafoline A (1) and its 6,6' -dirnethoxyl analog 2 were synthesized via the resolution of their corresponding camphorsulfonates of the racemates. The absolute configurations of (+)-1, (+)-2 and (-)-I, (-)-2 were assigned as (aR) and (aS), respectively, by the X-ray analysis and CD spectrum.
π SIMILAR VOLUMES
Optically active 1,1,2-trifluoro-or 1,2-difluoroallylic alcohols were prepared via a lipase-catalyzed reaction and their absolute configuration was determined by an X-ray crystallographic analysis of the corresponding ferrocene ester along with the refined Mosher method (the Kusumi-Ohtani method).
A route to 1,2\_dihydropyridines &-substituted with chiral auxiliaries has been developed starting from commercially available chiral amines. Cycloaddition between these dihydropyridines and methyl acrylate gave, in moderate d.e., isoquinuclidines of good enantiomeric purity whose absolute configura