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- W2556363070 endingPage "202" @default.
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- W2556363070 abstract "Domino reactions of 3‐acylchromones, namely 3‐methoxalyl‐, 3‐aroyl‐ and 3‐cinnamoylchromones, with heterocyclic ketene aminals (HKAs) proceed by attack of the nucleophile on the C‐2 atom of the chromone moiety, pyrone ring‐opening and subsequent formal [3+3] cyclocondensation with formation of functionalized tetracyclic fused chromeno[2,3‐ b ]pyridines or 2 H ,3 H ‐imidazo[1,2‐ a ]pyridines. The product distribution depends on the type of acyl group located at the 3‐position of the chromone and on the size of the heterocyclic moiety of the HKAs. The products show considerable activity as selective phosphatase inhibitors." @default.
- W2556363070 created "2016-11-30" @default.
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- W2556363070 creator A5080105809 @default.
- W2556363070 creator A5084933631 @default.
- W2556363070 date "2017-01-03" @default.
- W2556363070 modified "2023-10-16" @default.
- W2556363070 title "Reactions of 3-Acylchromones with Heterocyclic Ketene Aminals: One-Pot Synthesis and Phosphatase Inhibitory Activity of Fused Pyridine Derivatives" @default.
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