16547-35-6Relevant academic research and scientific papers
Synthesis of α-pyridone-based azaheteroaromatics by intramolecular vinylketene cyclizations onto the C=N bond of nitrogen heteroaromatics
Gurski Birchler,Liu,Liebeskind
, p. 7737 - 7745 (2007/10/02)
Substituted quinolizin-4-ones and ring-fused α-pyridone derivatives have been synthesized by the construction of 2,3-disubstituted-4-(2-azaheteroaryl)-2-cyclobutenones followed by thermal rearrangement. 4-(2-Azaheteroaryl)-2-cyclobutenones have been prepared regioselectively by the addition of 2-lithioazaheteroaromatics to cyclobutenediones and by palladium catalyzed cross-coupling of 4-chloro-2-cyclobutenones with 2-tri-n-stannylazaheteroaromatics. The thermal transformation is proposed to occur by ring-opening of the cyclobutenone followed by intramolecular cyclization of the transient vinylketene onto the carbon-nitrogen double bond of the azaheteroaromatic. A variety of quinolizin-4-ones, imidazo[1,2-a]pyridin-5-ones, 1-oxopyrido[2,1-b]benzothiazoles, and thiazolo[3,2-a]pyridin-5-ones were prepared.
A synthesis of highly substituted aromatics through regiocontrolled construction of cyclobutenones bearing unsaturated substituents at the 4-position
Krysan, Damian J.,Gurski, Angela,Liebeskind, Lanny S.
, p. 1412 - 1418 (2007/10/02)
2,3-Substituted 4-chloro-2-cyclobutenones, prepared by regiospecific transformations of substituted cyclobutenediones, undergo palladium-catalyzed cross-coupling with vinyl- and arylstannanes and vinylzirconium reagents to form 4-Runsat-2-cyclo
