1210053-75-0Relevant articles and documents
Synthesis of tetrahydro-5-azaindoles and 5-azaindoles using Pictet-Spengler reaction - Appreciable difference in products using different acid catalysts
Shumaila, Abdullah M.A.,Puranik, Vedavati G.,Kusurkar, Radhika S.
experimental part, p. 936 - 942 (2011/03/19)
Pictet-Spengler condensation of 2-(aryl)-2-(1H-pyrrol-2-yl)ethanamines using conventional acid catalysts like TMSCl or TFA resulted in the formation of substituted 5-azaindoles involving a tandem one pot four steps reaction sequence. By contrast use of gl
Microwave-assisted conjugate addition of pyrrole on electron-deficient nitro-olefins
Kusurkar, Radhika S.,Alkobati, Nabil A. H.
experimental part, p. 320 - 327 (2010/03/30)
Michael addition of pyrrole to-nitrovinyl compounds were carried out using microwave methodology. Monosubstituted pyrroles were obtained selectively in a major amount. Formation of novel product obtained during one of the reactions was explained by the double addition to nitrostyrene.