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- W2028721000 abstract "Abstract The intramolecular ene reaction of the 1,6-diene on a bicyclo[3.2.1]octane framework proceeds in a highly diastereoselective manner to form a trisubstituted pyrrolidine on the pyran ring in excellent yield. Its stereochemistry has been determined unambiguously by converting it into the known compound serving as a key intermediate of (−)-kainic acid." @default.
- W2028721000 created "2016-06-24" @default.
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- W2028721000 date "2010-05-23" @default.
- W2028721000 modified "2023-09-22" @default.
- W2028721000 title "ChemInform Abstract: Intramolecular Ene Reaction on a Bicyclo[3.2.1]octane System: An Alternative Route to (-)-Kainic Acid." @default.
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- W2028721000 doi "https://doi.org/10.1002/chin.200203199" @default.
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