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- W2000499536 abstract "[figure: see text] A new rearrangement of functionalized methoxy glycosides and a regioselective as well as stereoselective intramolecular Michael addition giving delta-valerolactones and C-glycosides are described. Applications to the synthesis of marine natural products are reported. Chemoselective deprotection of benzylated hydroxy groups is assumed to be facilitated by 6-endo-tet interaction with the 1,3-dithiane functionality." @default.
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- W2000499536 title "Versatile 8-Oxabicyclo[3.2.1]oct-6-en-3-one: Stereoselective Methodology for Generating<i>C</i>-Glycosides, δ-Valerolactones, and Polyacetate Segments" @default.
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- W2000499536 doi "https://doi.org/10.1021/ol006737a" @default.
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