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- W2890976930 endingPage "5968" @default.
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- W2890976930 abstract "An intramolecular Diels-Alder reaction of a silyl-substituted vinylimidazole delivers a diastereomeric mixture of C4-silyl functionalized dihydrobenzimidazoles. Subsequent diastereoselective reduction and elaboration of the lactone gives rise to a polysubstituted tetrahydrobenzimidazole, which, upon oxidative rearrangement, affords a single spirofused imidazolone containing all of the relevant functionality for an approach to the oroidin dimers axinellamine, massadine, and palau'amine." @default.
- W2890976930 created "2018-09-27" @default.
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- W2890976930 date "2018-09-07" @default.
- W2890976930 modified "2023-09-23" @default.
- W2890976930 title "Intramolecular Diels–Alder Reaction of a Silyl-Substituted Vinylimidazole en Route to the Fully Substituted Cyclopentane Core of Oroidin Dimers" @default.
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- W2890976930 doi "https://doi.org/10.1021/acs.orglett.8b02675" @default.
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