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- W2023361578 endingPage "2710" @default.
- W2023361578 startingPage "2710" @default.
- W2023361578 abstract "An expedient approach for the synthesis of various fused triazoles with varying functionality has been developed successfully via palladium catalysis in ligand free conditions. It was found that the additive TBAI greatly facilitates this palladium catalyzed cyclization to achieve the previously inaccessible fused triazolo[4,5-d]quinoline/chromene/thiochromene derivatives. This method provides a fast and simple access to obtain the fused triazoles in good to excellent yields. The synthesized compounds were screened with different cancer cell lines and the results has shown that compound 2a and 2f acts as inhibitors against specific non-small cell lung cancer cell line." @default.
- W2023361578 created "2016-06-24" @default.
- W2023361578 creator A5014310791 @default.
- W2023361578 creator A5032122455 @default.
- W2023361578 creator A5048997411 @default.
- W2023361578 creator A5069276976 @default.
- W2023361578 creator A5074235662 @default.
- W2023361578 creator A5091586049 @default.
- W2023361578 date "2013-01-01" @default.
- W2023361578 modified "2023-10-18" @default.
- W2023361578 title "Synthesis of fused triazolo[4,5-d]quinoline/chromene/thiochromene derivatives via palladium catalysis mediated by tetrabutylammonium iodide" @default.
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- W2023361578 doi "https://doi.org/10.1039/c2ra22799a" @default.
- W2023361578 hasPublicationYear "2013" @default.