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- W2951036557 abstract "A stereoselective synthesis of all functionalized C2–C10 fragment 13 of the antitumor marine natural product clavulactone was accomplished, starting from the commercially available 3-methylglutaric acid anhydride. Desymmetrization of 3-methylglutaric acid anhydride with (S)-α-phenylethanamine was successfully employed as a key step to embed the isolated C8-methyl group with the correct absolute configuration (99% de). The C3–C4 cis-double bond was stereospecifically furnished by an RCM (ring-closing metathesis) approach. Fragment 13 contains all preset functionalities and will be a useful precursor for the convergent total synthesis of clavulactone." @default.
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- W2951036557 date "2009-01-01" @default.
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- W2951036557 title "Stereoselective Synthesis of the Functionalized C2-C10 Fragment of Clavulactone" @default.
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- W2951036557 doi "https://doi.org/10.1002/cjoc.200990006" @default.
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