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- W2317994467 abstract "This communication describes the synthesis of the fully functionalized C1 to C13 segment (southern part) of highly potent cytotoxic marine natural product mandelalide A. Pd-catalyzed oxa-Michael cyclization followed by stereoselective reduction of the C7-ketone were carried out to construct the tetrahydropyran unit with required stereochemistry. The α,β-unsaturated ester moiety was constructed via cross-metathesis and the vinyl iodide was installed through modified Takai olefination." @default.
- W2317994467 created "2016-06-24" @default.
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- W2317994467 date "2016-01-11" @default.
- W2317994467 modified "2023-09-27" @default.
- W2317994467 title "Synthesis of the C1–C13 Fragment of Mandelalide A" @default.
- W2317994467 doi "https://doi.org/10.1055/s-0035-1561319" @default.
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