105224-04-2Relevant articles and documents
Use of activated enol ethers in the synthesis of pyrazoles: Reactions with hydrazine and a study of pyrazole tautomerism
Tarabova, Denisa,Soralova, Stanislava,Breza, Martin,Fronc, Marek,Holzer, Wolfgang,Milata, Viktor
supporting information, p. 752 - 760 (2014/05/06)
Activated enol ethers derived from esters or the dinitrile of malonic acid, or from pentane-2,4-dione were treated with hydrazine hydrate. The structures of the obtained products - pyrazoles 5 - were studied with a focus on tautomerism and supramolecular structure. A reverse addition of the reagents led to the isolation of two novel products, namely bis-enehydrazines 6 with an unsymmetrical arrangement of the formally equivalent subunits.
Reaction of 3-Benzylidene-2,4-pentanedione and 3-Methoxymethylene-2,4-pentanedione with Aroylhydrazines
Mitkidou, Sophia,Stephanidou-Stephanatou, Julia,Stephopoulou, Helen
, p. 441 - 444 (2007/10/02)
Aroylhydrazines 2 reacted with 3-benzylidene-2,4-pentanedione (1) to give 1-aroyl-3,5-dimethyl-1H-pyrazoles 5 and benzaldehyde aroylhydrazones 6. From the reaction of 3-methoxymethylene-2,4-pentanedione (7) with aroylhydrazines 2 the unknown N-aroyl-4-acetyl-1H-pyrazoles 9 were exclusively isolated in good yields.