591248-54-3Relevant articles and documents
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,
Tandem Diels-Alder cyclization/aromatization reactions of 5-vinyl-1-acyl-2-aryl-2,3-dihydro-4-pyridones
Kuethe, Jeffrey T.,Comins, Daniel L.
, p. 4179 - 4182 (2007/10/03)
A tandem Diels-Alder cyclization/aromatization of 5-vinyl-2,3-dihydro-4-pyridones and various dienophiles is reported. The intermediate Diels-Alder cycloadduct undergoes an elimination/aromatization to provide β-amino-ketones, β-amino-alcohols, and unnatu