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- W2950878441 abstract "Cycloaddition of 3,4-dibromofuran with azo diesters proceeds by a Diels–Alder reaction followed by a novel rearrangement to give 3,5-dibromotetrahydropyridazin-4-ones. Variable-temperature NMR spectroscopy shows four separate conformations at low temperature attributed to restricted rotation about the carbamate functions. The ethyl compound decomposes upon storage with loss of the carbamate groups and aromatisation to give a simple bromohydroxypyridazinium salt." @default.
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- W2950878441 date "2016-06-01" @default.
- W2950878441 modified "2023-09-27" @default.
- W2950878441 title "ChemInform Abstract: Novel Reaction of 3,4-Dibromofuran with Azo Diesters to Give Tetrahydropyridazinones." @default.
- W2950878441 cites W2281752179 @default.
- W2950878441 doi "https://doi.org/10.1002/chin.201628203" @default.
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