Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: synthesis of functionalized pyrrole derivatives.
Kou Hiroya, Shigemitsu Matsumoto, Masayasu Ashikawa, Kentaro Ogiwara, Takao Sakamoto
文献索引:Org. Lett. 8(23) , 5349-52, (2006)
全文:HTML全文
摘要
[Structure: see text] PtCl4-catalyzed cyclization reactions of homopropargyl azide derivatives to pyrrole rings were investigated. Using ethanol as solvent with 2,6-di-tert-butyl-4-methylpyridine as the base was found to be the best set of conditions for effecting this ring-closing reaction. These reaction conditions can be applied to the preparation of functionalized pyrrole derivatives, with no effect on the functional groups.
相关化合物
相关文献:
2002-07-24
[J. Am. Chem. Soc. 124(29) , 8528-9, (2002)]
1995-01-15
[J. Org. Chem. 65(3) , 801-5, (2000)]
2014-06-25
[Chem. Commun. (Camb.) , (2014)]
[Synthesis , 283, (1980)]
[Organic Synth. 68 , 138, (1990)]