Asymmetric synthesis of 1,2-amino alcohols using tert-butanesulfinimines as chiral auxiliary
Facile and highly stereoselective synthesis of 1,2-amino alcohols has been achieved by the addition of [(dimethylphenylsilyl)methyl] magnesium chloride to the tert-butanesulfinimines, followed by Fleming-Tamao oxidation of the silicon moiety.
- Publisher
- Georg Thieme Verlag Kg
- Issue Date
- 2005-02
- Language
- English
- Article Type
- Article
- Keywords
BETA-AMINO ALCOHOLS; HYDROGEN-PEROXIDE OXIDATION; ORGANIC-SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; SILAFUNCTIONAL COMPOUNDS; ENANTIOSELECTIVE SYNTHESIS; CARBON BOND; ACIDS; INHIBITOR; IMINES
- Citation
SYNLETT, no.2, pp.304 - 308
- ISSN
- 0936-5214
- Appears in Collection
- Files in This Item
- There are no files associated with this item.
This item is cited by other documents in WoS
| ⊙ Detail Information in WoSⓡ | Click to see |  |
| ⊙ Cited 8 items in WoS | Click to see citing articles in |  |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.