1234371-06-2Relevant academic research and scientific papers
Synthesis of polysubstituted pyrroles in aqueous medium directly from nitro compounds
Madhava Reddy, L.,Chandrashekar, P.,Reddy, A. R.,Reddy, C. K.
, p. 155 - 161 (2015)
A novel approach for the synthesis of polysubstituted pyrroles has been followed through multicomponent reaction of nitro compounds, phenacyl bromide or its derivatives and dialkyl acetylene dicarboxylates using indium in dilute aqueous HCl at room temperature. The products are formed in high yields (75-87%) in 10-16 h.
Novel and efficient supramolecular synthesis of pyrroles in the presence of β-cyclodextrin in water
Ramesh,Karnakar,Satish,Nageswar
, p. 1331 - 1334 (2013/02/22)
A simple and efficient synthesis of highly substituted pyrroles was achieved in water medium via multi-component strategy, using amine, DMAD/DEAD as well as phenacyl bromide catalyzed by β-CD. Utilizing this protocol various pyrrole derivatives were synthesized in good to excellent yields.
An efficient new method for the synthesis of polysubstituted pyrroles
Das, Biswanath,Reddy, Gandolla Chinna,Balasubramanyam, Penagaluri,Veeranjaneyulu, Boyapati
experimental part, p. 1625 - 1628 (2010/06/19)
The three-component reactions of phenacyl bromide or its derivatives, amine, and dialkyl acetylenedicarboxylate in the presence of iron(III) chloride as a catalyst at room temperature afforded polysubstituted pyrroles in high yields. Georg Thieme Verlag Stuttgart.
