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- W2951710347 abstract "Abstract An efficient and practical copper-catalyzed consecutive synthesis of quinazolin-4(3 H )-ones and pyrido[2,3- d ]pyrimidin-4(3 H )-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 S N Ar, reduction, cyclization, and oxidation. Notably, this work would provide a novel synthetic strategy for bioactive molecules containing quinazolinone class skeletons." @default.
- W2951710347 created "2019-06-27" @default.
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- W2951710347 date "2016-05-01" @default.
- W2951710347 modified "2023-10-18" @default.
- W2951710347 title "ChemInform Abstract: Copper-Catalyzed Consecutive Reaction to Construct Quinazolin-4(3H)-ones and Pyrido[2,3-d]pyrimidin-4(3H)-ones." @default.
- W2951710347 cites W2202022332 @default.
- W2951710347 doi "https://doi.org/10.1002/chin.201624177" @default.
- W2951710347 hasPublicationYear "2016" @default.
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