New Fluorinated 1,3-Vinylogous Amidines as Versatile Intermediates: Synthesis of Fluorinated Pyrimidin-2(1H)-ones.
β Scribed by Santos Fustero; Julio Piera; Juan F. Sanz-Cervera; Raquel Roman; Benjamin H. Brodsky; Maria Sanchez-Rosello; Jose Luis Acena; Carmen Ramirez de Arellano
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 26 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
New derivatives of 1,2-dihydro-2-alkenyl-3H-pyrazoC 3-ones 6 and 7 have been synthesized at room temperature by a one-pot two-step reaction of PCZ,, a ketone methylhydrazone, and a f3-keto ester. With ketone methylhydrazones bearing at least a phenyl group in the a-positions to the C=N bond and in t
## Abstract A series of novel 1βphenylthieno[1,2,4]triazolo[4,3β__a__]pyrimidinβ5(4__H__)βone derivatives **5** and **6** were synthesized by oxidative cyclization of thienopyrimidinonyl hydrazones using iodobenzene diacetate. J. Heterocyclic Chem., (2011).