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- W2023536443 abstract "Alkyl halides, including heteroarylmethyl and arylmethyl halides, bromoacetate, and cinnamyl bromide, are readily prepared via halogenation from basic raw materials, even using green processes. It is essential to replace their downstream products with them to prepare medicinally important heterocycles quinazolin-4(3H)-ones. Copper(I) bromide catalyzed domino reaction of alkyl halides and anthranilamides under air affords 2-substituted quinazolin-4(3H)-ones in good to excellent yields and with wide functional group tolerance. A mechanism for a copper(I) bromide involved organometal-catalyzed reaction via a four-step domino reaction is proposed." @default.
- W2023536443 created "2016-06-24" @default.
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- W2023536443 date "2014-05-22" @default.
- W2023536443 modified "2023-09-23" @default.
- W2023536443 title "ChemInform Abstract: Copper-Catalyzed Domino Synthesis of Quinazolin-4(3H)-ones from (Hetero)arylmethyl Halides, Bromoacetate, and Cinnamyl Bromide." @default.
- W2023536443 cites W2951485718 @default.
- W2023536443 doi "https://doi.org/10.1002/chin.201423181" @default.
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