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- W2108754878 abstract "A stereocontrolled synthesis of the C1-C9 segment of the marine natural product peloruside A is described. The key steps involve Sharpless's catalytic asymmetric dihydroxylation reaction, a chelation-controlled reduction of chiral β-alkoxy ketones to elaborate the syn-1,3-diol functionality and a ring-closing olefin metathesis of a homoallylic alcohol-derived acrylate ester to form an α,β-unsaturated δ-lactone." @default.
- W2108754878 created "2016-06-24" @default.
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- W2108754878 date "2003-05-01" @default.
- W2108754878 modified "2023-10-05" @default.
- W2108754878 title "An enantioselective synthesis of the C1C9 segment of antitumor macrolide peloruside A" @default.
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- W2108754878 doi "https://doi.org/10.1016/s0040-4039(03)00744-5" @default.
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