42046-68-4Relevant academic research and scientific papers
Synthesis of 2,3-dicarbonylated pyrroles and furans via the three-component Hantzsch reaction
Moss, Thomas A.,Nowak, Thorsten
experimental part, p. 3056 - 3060 (2012/08/08)
Pyrroles containing a 2,3-dicarbonyl substitution pattern are synthesized in one step via a three-component Hantzsch procedure. The normally difficult-to-access substrates are readily obtained in short reaction times and in moderate to good yields, giving pharmaceutically attractive products containing multiple handles for further elaboration.
(E)-3-(2-(N-phenylcarbamoyl)vinyl)pyrrole-2-carboxylic acid derivatives. A novel class of glycine site antagonists
Balsamini, Cesarino,Bedini, Annalida
, p. 808 - 820 (2007/10/03)
The synthesis and preliminary biological evaluation of novel (E)-3-(2- (N-phenylcarbamoyl)-vinyl)pyrrole-2-carboxylic acids bearing alkyl, acyl, alkoxy, phenyl, and halo substituents at the 4- and 5-positions of the pyrrole ring are reported. These compou
