105357-89-9Relevant articles and documents
Efficient synthesis of substituted pyrroles through iron-mediated oxidation reaction of 3-methylenehexane-2,5-dione with primary amines
Chen, Xi,Yuan, JiaCheng,Zhou, Min
, p. 32 - 38 (2018/12/11)
An efficient route has been developed for the synthesis of multiple substituted pyrrole derivatives from the readily available agents through iron-mediated oxidative aromatization process in good to excellent yields. This method is well tolerated with a diverse broad range of substrates and a complementary approach to currently available synthetic methods.
Silver-catalysed hydroamination: Synthesis of functionalised pyrroles
Robinson, Ross S.,Dovey, Martin C.,Gravestock, David
, p. 6787 - 6789 (2007/10/03)
It has been shown that functionalised pyrroles can be efficiently prepared using a two-step sequence. This sequence involves the propargylation of secondary enaminones using n-BuLi and propargyl bromide, followed by intramolecular hydroamination catalysed by silver nitrate. The hydroamination can be carried out at room temperature (overnight) or in a domestic microwave oven (60 s).
Gold-Catalyzed Sequential Amination/Annulation Reactions of 2-Propynyl-1,3-dicarbonyl Compounds
Arcadi, Antonio,Di Giuseppe, Sabrina,Marinelli, Fabio,Rossi, Elisabetta
, p. 443 - 446 (2007/10/03)
The gold(III)-catalyzed sequential amination/annulation reaction of 2-propynyl-1,3-dicarbonyl compounds 1 with primary amines 2 produces 1,2,3,5-substituted pyrroles 4 in moderate to high yields.