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- W2949911344 abstract "A protected α-d-glucopyranosylacetaldehyde was converted by Wittig reaction with (thiazol-2-yl)carbonylmethylenetriphenyl phosphorane into the corresponding substituted 1-oxa-1,3-butadiene which by hetero-Diels-Alder reaction with ethyl vinyl ether afforded a mixture of two diastereoisomeric dihydropyran derivatives. These were separated by chromatography and the thiazol ring was transformed into an aldehyde group. Subsequent hydroboration afforded α-C-(1→3)-linked disaccharides containing 2-deoxyhexopyranoses of d- or l-configuration." @default.
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- W2949911344 date "2003-01-01" @default.
- W2949911344 modified "2023-10-17" @default.
- W2949911344 title "A Stereocontrolled Access to α-C-(1→3)-Linked DisaccharidesContaining 2-Deoxyhexopyranoses" @default.
- W2949911344 doi "https://doi.org/10.1055/s-2003-39288" @default.
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