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• W2950996530 endingPage "8727" @default.
• W2950996530 startingPage "8724" @default.
• W2950996530 abstract "The reaction of various 1,2,4-oxadiazoles with an excess of hydrazine in DMF has been investigated. 3-Amino-1,2,4-triazoles are produced through a reductive ANRORC pathway consisting of the addition of hydrazine to the 1,2,4-oxadiazole followed by ring-opening, ring-closure, and final reduction of the 3-hydroxylamino-1,2,4-triazole intermediate. The general applicability of 1,2,4-oxadiazoles ANRORC reactivity is demonstrated also in the absence of C(5)-linked electron-withdrawing groups." @default.
• W2950996530 created "2019-06-27" @default.
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• W2950996530 date "2010-11-16" @default.
• W2950996530 modified "2023-10-18" @default.
• W2950996530 title "Synthesis of Amino-1,2,4-triazoles by Reductive ANRORC Rearrangements of 1,2,4-Oxadiazoles" @default.
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• W2950996530 doi "https://doi.org/10.1021/jo102049r" @default.
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