58753-78-9Relevant academic research and scientific papers
Synthesis of functionalized β-enamino compounds by carbon-fragment transfer reaction of C(2)-substituted imidazolidines with amines
Zhang, Yongbin,Li, Donghong,Zhou, Guofu,Xia, Chizhong,Guo, Wei
, p. 1123 - 1131 (2008/12/20)
The substituted imidazolidines (2, 3, 5) and a ring-opening product, N,N,N'-trisubstituted 2-methyl-ethylenediamines (4), derived from addition of the carbon anions to 1-tosyl-3,4-dimethylimidazolinium iodide (1), were utilized to transfer substituted one-carbon units to various amines to yield a series of functionalized β-enamino compounds.
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
