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- W1971293727 abstract "5,5′-Diethyl- and 5-phenyldipyrromethanes participate in cycloadditions with azo- and nitrosoalkenes giving dipyrromethanes with side chains containing open chain oximes and hydrazones. By controlling reaction stoichiometry it is possible to get mono or 1,9-disubstituted derivatives. The reported methodology gave access to a range of dipyrromethanes with good structural features for various applications. It was demonstrated that reduction of dipyrromethanes containing α-oximino ester groups opens the way to new α-amino esters." @default.
- W1971293727 created "2016-06-24" @default.
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- W1971293727 date "2013-03-01" @default.
- W1971293727 modified "2023-10-18" @default.
- W1971293727 title "Functionalization of dipyrromethanes via hetero-Diels–Alder reaction with azo- and nitrosoalkenes" @default.
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- W1971293727 doi "https://doi.org/10.1016/j.tetlet.2013.01.032" @default.
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