503570-30-7Relevant articles and documents
Efficient and regioselective synthesis of functionalized pyrroles by cyclocondensation of 1,3-dicarbonyl dianions with α-azidoketones
Langer, Peter,Freifeld, Ilia
, p. 2668 - 2669 (2002)
The cyclocondensation of 1,3-dicarbonyl dianions with α-azidoketones regioselectively afforded 2-alkylidenepyrrolidines which were transformed into functionalized pyrroles by treatment with acid.
Synthesis of 2-alkylidenepyrrolidines and pyrroles by condensation of 1,3-dicarbonyl dianions with α-azidoketones and subsequent intramolecular Staudinger-aza-Wittig reaction
Freifeld, Ilia,Shojaei, Heydar,Langer, Peter
, p. 4965 - 4968 (2007/10/03)
The condensation of 1,3-dicarbonyl dianions with α-azidoketones afforded open-chained condensation products that were transformed into pyrroles by Staudinger-aza-Wittig reactions and the subsequent treatment with trifluoroacetic acid.