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- W2034312168 endingPage "2003" @default.
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- W2034312168 abstract "The synthesis of crystalline per-O-TBS-beta-D-galactofuranose (4beta) as a new precursor of D-Gal f units is described. Anomeric iodination by reaction with TMSI followed by in situ coupling with simple alcohols and a wide variety of glycosyl acceptors, in the absence of a promoter, was employed as a new efficient glycosylation method for the assembly of D-galactofuranosyl moieties with high beta-stereoselectivity. Under the mild conditions of this reaction labile protective groups, like acetals, and furanosyl linkages are preserved." @default.
- W2034312168 created "2016-06-24" @default.
- W2034312168 creator A5024816654 @default.
- W2034312168 creator A5052643795 @default.
- W2034312168 date "2009-02-12" @default.
- W2034312168 modified "2023-10-08" @default.
- W2034312168 title "Facile Synthesis of per-<i>O-tert</i>-Butyldimethylsilyl-β-<scp>d</scp>-galactofuranose and Efficient Glycosylation via the Galactofuranosyl Iodide" @default.
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- W2034312168 doi "https://doi.org/10.1021/jo8025274" @default.
- W2034312168 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19215102" @default.
- W2034312168 hasPublicationYear "2009" @default.