173606-63-8Relevant academic research and scientific papers
Diels-Alder Reactions of N-acyl-2-alkyl(aryl)-5-vinyl-2,3-dihydro-4- pyridones
Comins, Daniel L.,Kuethe, Jeffrey T.,Miller, Teresa M.,Fevrier, Florence C.,Brooks, Clinton A.
, p. 5221 - 5234 (2007/10/03)
Readily available N-acyl-5-vinyl-2,3-dihydro-4-pyridones undergo Diels-Alder cyclization with various dienophiles to afford novel octahydroquinolines containing synthetically useful functionality. With dihydropyridone 5 and cis-disubstituted dienophiles,
Regiospecific substitution of N-acyl-2,3-dihydro-4-pyridones at C-5 via halogenation and cross-coupling
Comins,Comins, Daniel L.,Joseph,Joseph, Sajan P.,Chen,Xinghai, Chen
, p. 9141 - 9144 (2007/10/02)
The C-5 position of N-acyl-2-alkyl-2,3-dihydro-4-pyridones can be substituted by halogenation followed by a cross-coupling or carbonylation reaction.
