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- W1968305858 abstract "The tetracyclic epoxide 16 was prepared in stereocontrolled fashion from 4,4-dimethylcyclohexanone, the key steps being Saegusa ring expansion of its silyl enol ether to 5, ortho ester Claisen rearrangement of 7, and cyclization of 9 without rupture of the three-membered ring. Epoxide 16 had previously been transformed into dactylol, thus completing the formal total synthesis." @default.
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- W1968305858 title "A formal total synthesis of dactylol" @default.
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- W1968305858 doi "https://doi.org/10.1016/s0040-4039(01)80832-7" @default.
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