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- W2026789198 abstract "Nucleophilic opening of 1,2,5-orthoesters 1, 2 and 6 of D-arabinose with alcohols, ethanethiol and selenophenol was carried out under very mild conditions with Lewis acid catalysis. The reaction is stereoselective and gave α-D-arabinofuranosides in high yields. Various monoarabinofuranosides, thio- and selenoglycoside donors as well as acceptors were obtained in few steps from the opening products. These building blocks define a comprehensive system of glycosylation for the synthesis of any glycosidic linkage between arabinofuranosides. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)" @default.
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- W2026789198 date "2002-11-01" @default.
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- W2026789198 title "Elaboration of Monoarabinofuranosidic Building Blocks" @default.
- W2026789198 doi "https://doi.org/10.1002/1099-0690(200211)2002:22<3864::aid-ejoc3864>3.0.co;2-8" @default.
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