A simple and convenient synthesis of tautomeric (6 or 2)-hydroxy-4-methyl-(2 or 6)-oxo-1-(substituted phenyl)-(1,2 or 1,6)-dihydropyridine-3-carbonitriles
✍ Scribed by Ajaj, Ismail; Mijin, DuÅ¡an; Maslak, Veselin; BrkoviÄ, Danijela; MilÄiÄ, MiloÅ¡; TodoroviÄ, Nina; MarinkoviÄ, Aleksandar
- Book ID
- 120217315
- Publisher
- Springer Vienna
- Year
- 2013
- Tongue
- English
- Weight
- 435 KB
- Volume
- 144
- Category
- Article
- ISSN
- 0026-9247
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The 6-methoxy and 6tetrahydropyranyloxy-2,3-&hy~1,4-benxdoxms can be bthmted at the Sposmon to give mtermdate hth~o darvahves wbch react with various electrophrles to affod, after hydrolys~, S-substMed-&methoxy and 6-hydroxy-2.3~ydro-1.4-ben~oxtns
## Abstract The 1,3‐dipolar addition reaction of acrylonitrile to the betaine 1‐phenyl or methyl‐3‐oxidopyridinium is not so highly regioselective as generally assumed. New regioisomers are isolated. Their structures are proven by mass spectroscopy and proton‐and carbon‐NMR spectroscopy. Some 3,4di