## Abstract magnified image The phenylhydrazones **1aβd** condensed with ethyl cyanoacetate to yield pyridazinones **2aβd** that reacted with sulphur in presence of piperidine to yield the aminothienopyridazineones **3a,b** that reacted with electron poor olefins and acetylenes to yield phthalazin
Microwaves in Organic Synthesis: Synthesis of Pyridazinones, Phthalazinones and Pyridopyridazinones from 2-Oxo-arylhydrazones under Microwave Irradiation.
β Scribed by Balkis Al-Saleh; Noha M. Hilmy; Morsy Ahmed El-Apasery; Mohamed H. Elnagdi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 30 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Several .3(2H)-pyridazinones 4 were prepared from monophenvlhydrazones of 1,2 dicarbonyl compounds 1 and various active methylene compounds 2 within 1-15 minutes, without solvent, under microwave irradiation, in the presence of carefully adjusted amounts of piperidine or solid potassium t-butoxide.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract For Abstract see ChemInform Abstract in Full Text.