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- W2952389290 abstract "Abstract To take advantage of synthetic intermediates on the way to KDO, we developed a new strategy based on an aqueous hetero Diels-Alder reaction with a water-soluble diene derived from D-glyceraldehyde, followed by a dihydroxylation of the newly created double bond. The stereoselectivities of these reactions were investigated to give rise to 2-deoxy-KDO, which was sulfenylated via the enolate to yield β-thioglycoside, the hydrolysis of which led to KDO." @default.
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- W2952389290 date "2010-08-20" @default.
- W2952389290 modified "2023-09-26" @default.
- W2952389290 title "ChemInform Abstract: New Strategy in the Synthesis of 3-Deoxy-D-manno-2-octulosonic Acid ( KDO), 2-Deoxy-KDO and Thioglycoside of KDO." @default.
- W2952389290 cites W2057194009 @default.
- W2952389290 doi "https://doi.org/10.1002/chin.199339278" @default.
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