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- W2912367725 endingPage "2688" @default.
- W2912367725 startingPage "2676" @default.
- W2912367725 abstract "A highly chemoselective reaction between 5-aminoisoxazoles and α-diazocarbonyl compounds has been described. Both Wolff rearrangement and N-H insertion products can be obtained selectively by the judicious choice of reaction conditions. In the case of the Wolff rearrangement reactions, the N-isoxazole amides are accessed as the sole products under thermal conditions. On the other hand, α-amino acid derivatives of N-isoxazolescan be obtained through N-H insertion reactions in the presence of catalytic Rh2(Oct)4. Both reactions proceed under mild reaction conditions and feature a broad substrate scope." @default.
- W2912367725 created "2019-02-21" @default.
- W2912367725 creator A5035805485 @default.
- W2912367725 creator A5036712305 @default.
- W2912367725 creator A5037694652 @default.
- W2912367725 creator A5042993027 @default.
- W2912367725 creator A5048340466 @default.
- W2912367725 creator A5060844794 @default.
- W2912367725 creator A5084452813 @default.
- W2912367725 date "2019-01-31" @default.
- W2912367725 modified "2023-10-16" @default.
- W2912367725 title "Reactions of 5-Aminoisoxazoles with α-Diazocarbonyl Compounds: Wolff Rearrangement vs N–H Insertion" @default.
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