Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin

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dc.contributor.authorMohammed A. Al-Nuri
dc.date.accessioned2016-09-07T10:16:47Z
dc.date.available2016-09-07T10:16:47Z
dc.date.issued1994
dc.description.abstractReaction of nitrone (V with a, f1 -unsaturated lactone C.4) resulted in the isolation of a single adduct (7). The observed high regiochemical control has encouraged further explorations of natural product synthesis. A route to the synthesis of an interesting member of Pyrrolizidine- Alkaloid family; (±) -Tussilagin 90/ has been described.en
dc.identifier1727-2114
dc.identifier.urihttp://hdl.handle.net/20.500.11888/1939
dc.titleAlpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilaginen
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An-Najah University Journal for Research - A (Natural Sciences)