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- W2956005171 abstract "Quinolinium salts, Q+-CH2-CO2Me Br- and Q+-CH2-CONMe2 Br- (where Q = quinoline), were prepared from quinolines. Deprotonation of these salts with triethylamine promoted the reaction of the resulting quinolinium ylides (formally azomethine ylides) with electron-poor alkenes by conjugate addition followed by cyclization or by [3 + 2] dipolar cycloaddition. The pyrroloquinoline products were formed as single regio- and stereoisomers. These could be converted to other derivatives by Suzuki-Miyaura coupling, reduction or oxidation reactions." @default.
- W2956005171 created "2019-07-12" @default.
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- W2956005171 date "2019-07-03" @default.
- W2956005171 modified "2023-09-25" @default.
- W2956005171 title "Synthesis of pyrrolo[1,2-<i>a</i>]quinolines by formal 1,3-dipolar cycloaddition reactions of quinolinium salts" @default.
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- W2956005171 doi "https://doi.org/10.3762/bjoc.15.149" @default.
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