Mononuclear heterocyclic rearrangements. Effect of the structure of the side chain on the reactivity. Part 1. Rearrangement of some 3-arylureines of 5-pheny-1,2,4-oxadiazole into 1-aryl-3-benzoylamino-1,2,4-triazolin-5-ones in acetonitrile, benzene, and dioxane

Mononuclear heterocyclic rearrangements. Effect of the structure of the side chain on the reactivity. Part 1. Rearrangement of some 3-arylureines of 5-pheny-1,2,4-oxadiazole into 1-aryl-3-benzoylamino-1,2,4-triazolin-5-ones in acetonitrile, benzene, and dioxane–water

Published:1990 Issue:8 Volume: Page:1289-1295
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Frenna Vincenzo,Spinelli Domenico,Consiglio Giovanni

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P2/P29900001289

Reference38 articles.

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4. A. J. Boulton , ‘Lectures in Heterocyclic Chemistry,’Hetero Corporation, Provo, 1973.

5. Mononuclear heterocyclic rearrangements. Part 14. Rearrangement of some Z-arylhydrazones of 3-benzoyl-5-phenylisoxazole to 2-aryl-4-phenacyl-1,2,3-triazoles in dioxane–water

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