58753-74-5Relevant academic research and scientific papers
Synthesis of α-aryl enaminones through reactions of β-aryl enones with benzyl azide
Cunha, Silvio,Gomes, Amenson Trindade
supporting information, p. 6710 - 6713 (2013/01/15)
Reaction of benzalacetones and dibenzalacetones with benzyl azide promoted by BF3·OEt2 afforded Z and E densely substituted acyclic α-aryl enaminones in 21-95% yield. For benzalacetones major Z-isomers were obtained, while E-isomers
NMR of enaminones: Part 8-1H, 13C and 17O NMR spectra of primary and secondary 1,2-disubstituted enaminones: Configuration, conformation and intramolecular hdydrogen bonding
Zhuo, Jin-Cong
, p. 565 - 572 (2007/10/03)
The 1H. 13C and 17O NMR spectra for four series of C-2-substituted enaminones are reported: MeCO(Me)C=CHNHR (1), EtCO(Me)=CHNHR (2), PhCO(Me)C=CHNHR (3) and MeCO(Me)C=CHNHR (4). The 1H, 13C and 1
