K5[PW11ZnO39].23H2O-catalyzed acylation/ring expansion of ketoaziridines in a single pot: a new regio- and stereo-selective route
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- 作者：Heshmat A. Samimi ; Akram Mostafavi…
- 关键词：Aziridine ; Ring expansion ; Oxazoline ; K5[PW11ZnO39].23H2O
- 刊名：Journal of the Iranian Chemical Society
- 出版年：2015
- 出版时间：November 2015
- 年：2015
- 卷：12
- 期：11
- 页码：2031-2035
- 全文大小：419 KB
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Akram Mostafavi (1)
Mostafa Riahi Farsani (2)
1. Department of Chemistry, Faculty of Sciences, The University of Shahrekord, P. O. Box 115, Shahrekord, Iran
2. Young Researchers and Elite Club, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran - 刊物主题：Analytical Chemistry; Inorganic Chemistry; Physical Chemistry; Biochemistry, general; Organic Chemistry;
- 出版者：Springer Berlin Heidelberg
- ISSN：1735-2428
文摘
A new and one-pot synthesis of oxazolines has been accomplished by K5[PW11ZnO39].23H2O—catalyst acylation followed by C–N ring opening/C–O bond formation in NH ketoaziridines. This regio- and stereo-selective reaction presumably proceeds via a domino sequence resulting in the in situ generation of acyl aziridine which undergoes a ring expansion reaction via an initial C–N rupture of aziridine ring followed by ring closure to the oxazolines. The methodology provided novel one-pot procedure for the synthesis of trans-2,5-diaryl-4-aroyloxazolines. Keywords Aziridine Ring expansion Oxazoline K5[PW11ZnO39].23H2O