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- W2934784895 abstract "The formal synthesis of Cladospolide-C and its analog is achieved by using enantiopure (R)-γ–valerolactone 10. The significant points of this synthesis are the stereoselective dihydroxylation of α, β-unsaturated ester 16 using Sharpless protocol, Wittig olefination of γ –valerolactol 6 with triphenylphosphonium iodide salt 7, one pot selective oxidation of 22 and subsequent C2-homologation with good E/Z ratio." @default.
- W2934784895 created "2019-04-11" @default.
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- W2934784895 date "2019-05-01" @default.
- W2934784895 modified "2023-10-16" @default.
- W2934784895 title "Formal synthesis of Cladospolide C & epi-Cladospolide C using R-(+)-γ-valerolactone as a chiral synthon" @default.
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- W2934784895 doi "https://doi.org/10.1016/j.tet.2019.04.001" @default.
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