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- W2202022332 endingPage "874" @default.
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- W2202022332 abstract "An efficient and practical copper-catalyzed consecutive synthesis of quinazolin-4(3H)-ones and pyrido[2,3-d]pyrimidin-4(3H)-ones from easily available 2-halobenzamides (or 2-halonicotinamides), aldehydes, and sodium azide has been developed, which gave the corresponding target products in 50–95% yields for 29 examples. This remarkable consecutive process involved sequential copper-catalyzed SNAr, reduction, cyclization, and oxidation. Notably, this work would provide a novel synthetic strategy for bioactive molecules containing quinazolinone class skeletons." @default.
- W2202022332 created "2016-06-24" @default.
- W2202022332 creator A5005228021 @default.
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- W2202022332 date "2016-02-01" @default.
- W2202022332 modified "2023-10-18" @default.
- W2202022332 title "Copper-catalyzed consecutive reaction to construct quinazolin-4(3H)-ones and pyrido[2,3-d]pyrimidin-4(3H)-ones" @default.
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- W2202022332 doi "https://doi.org/10.1016/j.tet.2015.12.059" @default.
- W2202022332 hasPublicationYear "2016" @default.
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