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- W2953236788 abstract "2,3-Benzannelated dipyrrinone analogs (1 and 2) of xanthobilirubic acid (3) are prepared by base-catalyzed condensation of isoindolinone (5) and indolin-2-one (6) respectively, with methyl 3-(2-formyl-3,5-dimethyl-1H-pyrrol-4-yl)propanoate (4). Nuclear Overhauser effect H-nmr studies indicate that both 1 and 2 adopt preferentially a syn-Z configuration. The former forms a hydrogen-bonded homodimer in nonpolar solvents; the latter is intramolecularly hydrogen bonded." @default.
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- W2953236788 date "2003-01-01" @default.
- W2953236788 modified "2023-10-14" @default.
- W2953236788 title "Syntheses and properties of benzodipyrrinones" @default.
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- W2953236788 doi "https://doi.org/10.1002/jhet.5570400127" @default.
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