Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5216491 | Tetrahedron | 2013 | 9 Pages |
Abstract
New methods for the synthesis of (E)-3-halo-2-styryl-4H-chromen-4-ones were established. The reaction of these compounds with hydrazine hydrate afforded new and unexpected 3(5)-aryl-5(3)-[2-(2-hydroxyphenyl)-2-hydrazonoethyl]-1H-pyrazoles, which upon acid hydrolysis gave 3(5)-aryl-5(3)-[2-(2-hydroxyphenyl)-2-oxoethyl]-1H-pyrazoles. The reaction mechanisms for these transformations, involving 1,6- followed by 1,4-conjugate additions, are discussed and the structures of all new compounds were established by NMR studies.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Joana P.A. Ferreira, Vera L.M. Silva, José Elguero, Artur M.S. Silva,