Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/34689
標題: Microwave accelerated cycloaddition reactions of nitrile oxides and allylic alcohols
作者: Lu, T.J.
陸大榮
Tzeng, G.M.
關鍵字: microwave;nitrile oxide;cycloaddition;allylic alcohol;isoxazoline;regioselectivity;1,3-dipolar cycloaddition;chemical-reactions;isoxazoline route;organic-synthesis;chemistry;chlorides;additions;ketones;beta
Project: Journal of the Chinese Chemical Society
期刊/報告no:: Journal of the Chinese Chemical Society, Volume 47, Issue 1, Page(s) 189-196.
摘要: 
The application of microwaves in promoting the cycloaddition reactions of allyl alcohols with nitrile oxides using a domestic microwave oven and a focused monomode microwave reactor have demonstrated that not only was the reaction time substantially reduced, but also the reaction yields were significantly improved over the conventional stirred reactions. Microwave irradiation alters the regioselectivity of the cycloaddition reaction which favors the non-hydrogen-bond directed cycloadduct, isoxazoline 4.
URI: http://hdl.handle.net/11455/34689
ISSN: 0009-4536
Appears in Collections:化學系所

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