The 2-N,N-Dibenzylamino Group as a Participating Group in the Synthesis of β-Glycosides
✍ Scribed by Hailong Jiao; Ole Hindsgaul
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 106 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0044-8249
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📜 SIMILAR VOLUMES
The Ferrier rearrangement of a galactal derivative 2 bearing the trichloroacetimidate functionality as a leaving group at the C-3 position was performed in the presence of trimethyl-
The N-DMM-Protected lactosamine derivative 2 was readily neohexaose). Glycosylation of acceptor 10 with donor 4 furnished tetrasaccharide 16 which, employing standard transformed into the corresponding glycosyl donor 4 and into acceptor 5. A TMSOTf-catalyzed glycosidation afforded the procedures, ga
## Abstract We have synthesized and examined the preferred conformation of a set of N‐benzhydryl‐glycolamide esters from N^α^‐protected (or N^α^‐blocked) α‐amino acids. Experiments were performed in CDCl~3~ solution by Fourier transform infrared absorption and ^1^H‐NMR techniques, and in the crysta