Abstract
The photocycloaddition of aldehydes and alpha-ketoesters to 2,5-dimethyl-4-isobutyloxazole leads to bicyclic oxetanes with high to moderate (exo) diastereoselectivity that can be easily ring-opened to give alpha-amino-beta-hydroxyketones.
- Title
- Diastereoselective photochemical synthesis of alpha-amino-beta-hydroxyketones by photocycloaddition of carbonyl compounds to 2,5-dimethyl-4-isobutyloxazole
- Creators - without role
- Samir Bondock - Mansoura UniversityAxel G. Griesbeck - University of Cologne
- Publication Details
- Monatshefte für Chemie, Vol.137(6), pp.765-777
- Publisher
- Springer Nature
- Number of pages
- 13
- Identifiers
- 9923130008331
- Academic Unit
- King Khalid University
- Language
- English
- Resource Type
- Journal article