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- W4379741974 abstract "Abstract Quinazolinedione derivatives were obtained from 2-aminobenzoic acids and bench-stable α-chloroaldoxime O-methanesulfonates via DMAP-catalyzed domino reactions under mild reaction conditions in one-pot fashion. Chemical transformations involved nucleophilic substitution, Tiemann rearrangement, and cyclic urea formation. The strength of nitrogen nucleophile of 2-aminobenzoic acids and the high level of carbon electrophile of α-chloroaldoxime O-methanesulfonates were crucial for the reaction outcome. An application to synthesize a quinazolinedione building block was introduced." @default.
- W4379741974 created "2023-06-08" @default.
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- W4379741974 date "2023-06-07" @default.
- W4379741974 modified "2023-09-26" @default.
- W4379741974 title "DMAP-Catalyzed Domino Reactions of α-Chloroaldoxime O-Methanesulfonates and 2-Aminobenzoic Acids for the Synthesis of Quinazolinediones" @default.
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- W4379741974 doi "https://doi.org/10.1055/a-2107-5653" @default.
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