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- W2047947186 abstract "The chiral aldehyde 7 was prepared by diastereoselective alkylation, subsequent 1,2- addition of isopropenylmagnesium bromide gave rise to a mixture (68:32) of the allylic alcohols 8 and 10 which was separated by recycling MPLC. Claisen rearrangement of the propionates of these alcohols under control of the enolate geometry finally yielded hydroxynonenoic acid 12b." @default.
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- W2047947186 title "Total syntheses of jaspamide (jasplakinolide) and geodiamolide A and B - 1. Stereoselective synthesis of (2,4,6,8)-8-hydroxy-2,4,6-trimethyl-4-nonenoicic acid1" @default.
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- W2047947186 doi "https://doi.org/10.1016/s0040-4039(00)80273-7" @default.
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