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- W1971910080 abstract "Epoxidation of triquinacene 3 with dimethyldioxirane proceeded with a high degree of exo-face selectivity to give a quantitative yield of a 1:1.5 mixture of all-exo-4a and endo,exo,exo-triepoxytriquinane 4b. Subsequent lithium aluminum hydride reduction of the all-exo-triepoxide 4a gave all-exo-2,5,8-5a and all-exo-2,5,9-trihydroxytriquinane 5b, respectively. The straightforward 3-fold dihydroxylation of triquinacene 3 led exclusively to the all-exo-hexahydroxytriquinane 8 in one step. X-ray crystal structure analyses confirmed the configuration of the triepoxide 4b and the hexaacetate 9 of the hexol 8." @default.
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- W1971910080 date "1998-03-28" @default.
- W1971910080 modified "2023-10-09" @default.
- W1971910080 title "Highly <i>Exo</i>-Selective Epoxidation and Hydroxylation of Triquinacene and Its Derivatives: <i>all</i>-<i>exo</i>-Hexahydroxytriquinane" @default.
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- W1971910080 doi "https://doi.org/10.1021/jo971796w" @default.
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