Expedient synthesis of tetrasubstituted pyrroles via a copper-catalyzed cascade inter-/intramolecular cyclization of 1,3-enynes carry a nitro group with amines.
Ganesan Bharathiraja, Mani Sengoden, Masanam Kannan, Tharmalingam Punniyamurthy
文献索引:Org. Biomol. Chem. 13(9) , 2786-92, (2015)
全文:HTML全文
摘要
Various tetrasubstituted pyrroles/pyrazoles have been prepared from nitro-substituted 1,3-enynes with aromatic amines/hydrazines via a copper-catalyzed cascade aza-Michael addition, cyclization and aromatization at room temperature. This protocol is also effective for the synthesis of tetrasubstituted pyrazoles in high yields.
相关化合物
相关文献:
2014-08-01
[J. Pharm. Biomed. Anal. 97 , 141-50, (2014)]
2015-06-26
[Biochem. Biophys. Res. Commun. 462 , 99-104, (2015)]
2015-12-01
[J. Mater. Sci. Mater. Med. 26 , 275, (2015)]
2014-01-01
[BMC Cancer 14 , 841, (2014)]
2015-08-01
[Chirality 27 , 523-31, (2015)]