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Автор Arán, Vicente J.
Автор Pérez, Miguel A.
Автор Soto, José L.
Дата выпуска 1984
dc.description The 2-amino-4,5-dihydrofuran-3,4-dicarbonitriles (1aâ f) were thermally aromatized to the 2-aminofuran-3-carbonitriles (2aâ f) which, in turn, underwent photoxidative ring transformation into the 2,5-dihydro-5-hydroxy-2-oxopyrrole-3-carbonitriles (3bâ e). Mild acidic hydrolysis of the 2-amino-4,5-dihydrofuran-3,4-dicarbonitriles (1aâ g) led to the tetrahydro-2-oxofuran-3,4-dicarbo-nitriles (4aâ g). The representative compound (4a) was converted into the 2,5-dihydro-2-oxofuran-3-carbonitrile (5) or further transformed into the 3,3a-dihydrofuro[3,4-c]pyrrole-1,4,6-trione (6).
Формат application.pdf
Издатель Royal Society of Chemistry
Название Ring transformation and reactions of 2-amino-4,5-dihydrofuran-3,4-dicarbonitriles
Тип research-article
DOI 10.1039/P19840002009
Electronic ISSN 1364-5463
Print ISSN 0300-922X
Журнал Journal of the Chemical Society, Perkin Transactions 1
Первая страница 2009
Последняя страница 2011

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