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- Publisher
- Wiley
- Copyright
- Copyright © 2007 Wiley Subscription Services, Inc., A Wiley Company
- ISSN
- 1600-5368
- eISSN
- 1600-5368
- DOI
- 10.1107/S1600536807023574
- Publisher site
- See Article on Publisher Site
Abstract
The title compound, C28H41NO6, was obtained by reduction of benzyl 2‐deoxy‐2‐(3,5‐di‐tert‐butylsalicylideneamino)‐α‐d‐glucopyranoside. The benzyl substituent is in an axial position, whereas the 3,5‐di‐tert‐butylsalicylamino substituent and the hydroxyl groups are in equatorial positions. The enantiomerically pure title compound is a potential O,N,O‐chelate ligand suitable as a precursor for chiral transition metal complexes. The absolute configuration was determined by NMR experiments.
Journal
Acta Crystallographica Section E – Wiley
Published: Jun 1, 2007