6533b82bfe1ef96bd128d549
RESEARCH PRODUCT
A Carbohydrate-Based Julia–Kocienski Reagent for Syntheses of Chain-Extended and C-Linked Saccharides
James A. BullHorst Kunzsubject
chemistry.chemical_compoundchemistryChain (algebraic topology)LyxoseStereochemistryReagentOrganic ChemistryRiboseEpimerSmiles rearrangementCarbohydrateCatalysisGluconolactonedescription
The carbohydrate-derived Julia–Kocienski reagent 2-{[(3aS,4S,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]methylsulfonyl}-1,3-benzothiazole (6) was prepared from d -ribose and investigated in the eponymous olefination. The base-promoted generation of the Julia anion induced a rearrangement to the corresponding l -lyxose epimer 2-{[(3aS,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]methylsulfonyl}-1,3-benzothiazole (12), which reacted readily with aldehydes and with a gluconolactone. The latter reaction furnished an exo-glycal-linked C-diglycoside.
year | journal | country | edition | language |
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2014-02-18 | Synthesis |