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- W1998124546 abstract "Abstract The reaction of β-chloroacrolein with 1 equiv of 2-aminophenol in DMF proceeds smoothly to afford 11-hydroxy derivative of chromenoquinoline in good yield. This single pot method allows for a rapid access to a variety of chromenoquinolines or oxepinoquinolines depending on the nature of β-chloroacrolein used. The structures were established by spectroscopic data and further confirmed by X-ray diffraction analysis. A plausible mechanism for this reaction has been proposed. The reaction seemed to proceed via a chloroimine species, whose intermediacy has been established, followed by the construction of the fused quinoline ring." @default.
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- W1998124546 date "2008-06-17" @default.
- W1998124546 modified "2023-09-25" @default.
- W1998124546 title "ChemInform Abstract: Revisiting the Reaction of β-Chloroacroleins with 2-Aminophenol: A New Observation." @default.
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- W1998124546 doi "https://doi.org/10.1002/chin.200825155" @default.
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