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- W1992737674 abstract "Abstract The first enantioselective total synthesis of rumphellaone A, a cytotoxic 4,5-seco-caryophyllane isolated from the gorgonian coral Rumphella antipathies, has been achieved from a known olefinic alcohol by a 16-step sequence involving Stork's epoxy nitrile cyclization as the key step to concomitantly install a cyclobutane ring and three contiguous stereogenic centers contained in the molecule." @default.
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- W1992737674 date "2012-06-01" @default.
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- W1992737674 title "Synthesis of rumphellaone A via epoxy nitrile cyclization" @default.
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- W1992737674 doi "https://doi.org/10.1016/j.tet.2012.04.035" @default.
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