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- W2950896842 abstract "A concise entry to the skeleton of the tremulane sesquiterpenes is described that culminated in the first enantioselective syntheses of tremulenediol A and tremulenolide A. The approach features a series of efficient transition metal-catalyzed reactions commencing with an enantioselective rhodium(II)-catalyzed intramolecular cyclopropanation followed by a regioselective allylic alkylation and a diastereoselective rhodium(I)-catalyzed [5+2] cycloaddition." @default.
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- W2950896842 date "2006-11-01" @default.
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- W2950896842 title "Enantioselective syntheses of tremulenediol A and tremulenolide A" @default.
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- W2950896842 doi "https://doi.org/10.1016/j.tet.2006.05.087" @default.
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