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- W3118448782 endingPage "1120" @default.
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- W3118448782 abstract "A simple, mild, eco-friendly, general, and convenient approach has been developed for the synthesis of structurally diverse 2-arylbenzothiazole derivatives from the reactions of 2-aminothiophenol and various aromatic aldehydes using camphor sulfonic acid a low cost, commercially available, efficient organo-catalyst in aqueous ethanol at room temperature. Under the same optimized conditions, a series of 2-arylbenzimidazoles was also synthesized starting from o-phenylenediamines and various aldehydes whereas synthesis of 3H-spiro[benzo[d]thiazole-2,3′-indolin]-2′-ones was accomplished from the reactions of 2-aminothiophenol and substituted isatins." @default.
- W3118448782 created "2021-01-18" @default.
- W3118448782 creator A5004349344 @default.
- W3118448782 creator A5013011305 @default.
- W3118448782 creator A5029636657 @default.
- W3118448782 creator A5030637244 @default.
- W3118448782 creator A5048681449 @default.
- W3118448782 date "2021-01-08" @default.
- W3118448782 modified "2023-10-16" @default.
- W3118448782 title "Camphor sulfonic acid catalyzed a simple, facile, and general method for the synthesis of 2-arylbenzothiazoles, 2-arylbenzimidazoles, and 3<i>H</i>-spiro[benzo[<i>d</i>]thiazole-2,3′-indolin]-2′-ones at room temperature" @default.
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