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The reaction of β‐aminoenones with substituted acetonitriles. Regiospecific synthesis of 2(1H)‐pyridones
Author(s) -
Alberola Angel,
Andrés Celia,
Ortega Alfonso González,
Pedrosa Rafael,
Vicente Martina
Publication year - 1987
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570240333
Subject(s) - acetonitriles , chemistry , malononitrile , acetonitrile , ethyl cyanoacetate , yield (engineering) , medicinal chemistry , nitrile , organic chemistry , catalysis , materials science , metallurgy
Unsymmetrically substituted β‐aminoenones react with malononitrile, cyanomethylphenylsulfone, benzoyl‐acetonitrile and ethyl cyanoacetate, in very mild conditions, to yield regiospecifically 3‐functionalized 2(1 H )‐pyridones in high yields.