A simple conversion of azlactones into indenones via H3PW12O40/Al2O3 catalyzed intramolecular Friedel–Crafts reaction
摘要:
A rapid and simple procedure for the synthesis of the indenone derivatives, N-(1-oxo-1H-inden-2-yl)benzamides, via intramolecular Friedel-Crafts (IFC) reaction of (Z)-4-arylidene-2-phenyl-5(4)-oxazolones (azlactones) catalyzed by H3PW12O40 supported on neutral alumina under microwave irradiation has been developed. The reaction is straightforward and allows easy isolation of the product. The catalyst could be re-used up to four times after simple filtration. (C) 2011 Elsevier Ltd. All rights reserved.
An Efficient, Simple, and Scaleable Domino Reaction to Diverse N-(1-Oxo-1H-inden-2-yl)benzamides Catalyzed by HPW@nano-SiO2 under Microwave Irradiation
A facile, efficient, and large-scale strategy for the synthesis of N-(1-oxo-1H-inden-2-yl)benzamide derivatives via domino reaction between aryl aldehydes, hippuric acid, and acetic anhydride catalyzed by HPW@nano-SiO 2 was accomplished undermicrowaveirradiation. The reaction conditions are very simple and offer easy isolation of the product. Moreover, the catalyst can be reused up to five times