ChemInform Abstract: Enantioselective Synthesis of Protected α-Aminoketones via Electrophilic Amination of α-Silylketones with an Oxaziridine.
✍ Scribed by Dieter Enders; Christine Poiesz; Reni Joseph
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Enantioselective Synthesis of α-Hydroxy Phosphonates via Oxidation with (Camphorsulfonyl)oxaziridines. -Chiral dichloro oxaziridines (OXA) are used for the enantioselective introduction of the hydroxy group to prochiral phosphonates. The (+)-reagent favors the formation of (S)-products. Phosphonate
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v