Recently we reported on the reactions of cyclic g-diketones and carbethoxycycloalkanones with compound I under basic catalysis. 2 In monoglyme, the products obtained were, invariably a mixture of tautomers arising from protonation of an initially formed 1,6-adduct. In DMSO the products were derivab
β¦ LIBER β¦
Reaction of piperidone enamines with methyl .beta.-vinylacrylate. A route to quinolines and isoquinolines
β Scribed by Danishefsky, S.; Cavanaugh, Robert
- Book ID
- 111860717
- Publisher
- American Chemical Society
- Year
- 1968
- Tongue
- English
- Weight
- 508 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-3263
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## Abstract The enaminones **1b,d,f** react with 4βphenylβ3βmethylβ5βpyrazoleamine **3a** to yield the pyrazole derivatives **4aβc** that cyclised readily on reflux in pyridine solution in presence of hydrochloric acid to yield the pyrazolo[1,5β__a__]pyrimidines **5aβc.** Similarly 3(5)βaminoβ1__H_