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- W136995768 endingPage "398" @default.
- W136995768 startingPage "374" @default.
- W136995768 abstract "Direct C–N bond-forming reactions using azodicarboxylates and other electrophilic nitrogen reagents have turned out to be a simple and straightforward approach for the synthesis of nitrogen-containing compounds. In this context, the highly enantioselective amination of active nucleophiles, such as enolsilanes, ketoesters, pyruvic acid derivatives and enecarbamates, by chiral Lewis acid catalysis has been developed. Direct α-amination of aldehydes and ketones by enamine catalysis has also been achieved with excellent enantioselectivity. Brønsted base catalysis has also proven to be powerful in the direct asymmetric catalytic amination of active nucleophiles, such as α-aryl substituted cyanoacetates and β-dicarbonyl compounds. In addition to the use of azo-compounds, few other electrophiles such as sulfonyl azides have been used successfully." @default.
- W136995768 created "2016-06-24" @default.
- W136995768 creator A5014955790 @default.
- W136995768 creator A5036602688 @default.
- W136995768 creator A5052144587 @default.
- W136995768 date "2012-01-01" @default.
- W136995768 modified "2023-09-27" @default.
- W136995768 title "6.14 C–N Bond Formation: α-Amination and α-Hydrazination of Carbonyl Compounds with DEAD and Related Compounds" @default.
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