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• W2127558569 startingPage "10181" @default.
• W2127558569 abstract "The direct approach: The title coupling reactions of N-aryl glycine esters with unmodified ketones occurred smoothly in the presence of tert-butyl hydroperoxide (TBHP) or 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) under mild conditions (see scheme). The oxidant used for CH activation determined the selectivity of the reactions for a particular type of ketone substrate." @default.
• W2127558569 created "2016-06-24" @default.
• W2127558569 creator A5006099744 @default.
• W2127558569 creator A5027978435 @default.
• W2127558569 date "2010-11-29" @default.
• W2127558569 modified "2023-10-18" @default.
• W2127558569 title "Cross-Dehydrogenative Coupling Reactions by Transition-Metal and Aminocatalysis for the Synthesis of Amino Acid Derivatives" @default.
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• W2127558569 doi "https://doi.org/10.1002/anie.201004940" @default.
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