Direct synthesis of pyrroles via a silver-promoted three-component reaction involving unusual imidazole ring opening
J Zeng, Y Bai, S Cai, J Ma, XW Liu
Index: Zeng, Jing; Bai, Yaguang; Cai, Shuting; Ma, Jimei; Liu, Xue-Wei Chemical Communications, 2011 , vol. 47, # 48 p. 12855 - 12857
Full Text: HTML
Citation Number: 17
Abstract
A novel silver-promoted three-component reaction toward the synthesis of multifunctionalized pyrroles has been developed. This reaction involves an unusual imidazole ring decomposition, presumably via 1, 5-isomerization and subsequent hydrolysis.
Related Articles:
Devinylation of N-vinylpyrroles using mercury (II) acetate
[Schmidt; Vasil'Tsov; Zorina; Ivanov; Mikhaleva; Trofimov Chemistry of Heterocyclic Compounds, 2012 , vol. 47, # 10 p. 1300 - 1303]
Formylation en serie arylpyrrolique
[Boukou-Poba, Jean-Paul; Farnier, Michel; Guilard, Roger Canadian Journal of Chemistry, 1981 , vol. 59, p. 2962 - 2967]
Transition metal catalyzed ring opening reactions of 2-phenyl-3-vinyl substituted 2H-azirines
[Padwa, Albert; Stengel, Thomas Tetrahedron Letters, 2004 , vol. 45, # 31 p. 5991 - 5993]
Synthese de pyrroles et d'oxazoles par pyrolyse de N-(hydroxy-2′ ethyl) amino-3 propenoate
[Pale-Grosdemange, Catherine; Chuche, Josselin Tetrahedron, 1989 , vol. 45, # 11 p. 3397 - 3414]
Expedient synthesis of 1-vinylpyrrole-2-carbaldehydes
[Mikhaleva, Al'bina I.; Zaitsev, Alexey B.; Ivanov, Andrey V.; Schmidt, Elena Yu.; Vasil'tsov, Alexander M.; Trofimov, Boris A. Tetrahedron Letters, 2006 , vol. 47, # 22 p. 3693 - 3696]