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Synthesis 2000; 2000(5): 681-690
DOI: 10.1055/s-2000-6399
DOI: 10.1055/s-2000-6399
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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or duplication of any kind, translating, preparation of microfilms, and electronic
data processing and storage.Intramolecular Cyclization of 1,2-bis(N-alkoxy-N-nitrosoamino)alkanes: A Unique Route to 4,5-Dihydro-1,2,3-triazole 2-Oxides
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)

1,2-Bis(N-alkoxy-N-nitroso)amines 7 obtained by nitrosation of the corresponding 1,2-bisalkoxyamines 4 were smoothly converted into 1-alkoxy-4,5-dihydro-1,2,3-triazole 2-oxides 8 under reflux in methanol in high yields. 4H-1,2,3-Triazole 2-oxides 9, a novel type of triazole oxides, and 2-hydroxy-2H-1,2,3-triazoles 10 were obtained by the reaction of 1-alkoxy-4,5-dihydro-1,2,3-triazole 2-oxides 8 with sodium methoxide.
1,2-bisalkoxyamines - 1,2-bis(N-alkoxy-N-nitroso)amines - 1,2-bis(nitrosohydroxylamines) - 1,2,3-triazole 2-oxides - intramolecular cyclization - nitrogen - nitrosation - heterocycles