86397-90-2Relevant academic research and scientific papers
Synthesis of highly substituted pyrroles via oxidative free radical reactions of β-aminocinnamates
Tsai, An-I.,Chuang, Che-Ping
, p. 2235 - 2239 (2007/10/03)
Oxidative free radical reactions of β-aminocinnamates are described. Imine radicals produced by tetra-n-butylammonium cerium(IV) nitrate (TBACN) oxidation of enamines undergo efficient addition to the C-C double bond of β-aminocinnamates. This TBACN media
Oxidative free radical reactions of enamino esters
Chuang, Che-Ping,Wu, Yi-Lung
, p. 1841 - 1847 (2007/10/03)
Oxidative free radical reactions of enamino esters are described. Electrophilic carbon-centered radicals produced by the cerium(IV) ammonium nitrate (CAN) oxidation of β-dicarbonyl compounds undergo efficient addition to the C-C double bond of enamino est
Hypervalent iodine in synthesis. 62: A tandem dimerization-cyclocondensation of enamine-esters with [bis(trifluoroacetoxy)iodo]benzene: A method of synthesis of highly substituted pyrroles
Zhang,Chen
, p. 1619 - 1624 (2007/10/03)
A tandem dimerization-cyclocondensation of enamine-esters with [bis(trifluoroacetoxy)iodo]benzene(BTI) provides an effective method for synthesis of highly substituted pyrroles.
OXIDATION OF ENAMINE-ESTERS WITH LEAD TETRA-ACETATE - PART 3. β-AMINOCINNAMATES AND β-AMINOCROTONATES
Sukari, Mohamed A.,Vernon, John M.
, p. 793 - 796 (2007/10/02)
Oxidation of β-aminocinnamates and β-aminocrotonates with lead tetra-acetate gives fully substituted pyrrole-3,4-diesters.
