Angewandte Chemie International Edition · 2012 · 70 citations · 19 references
Life SciencesBiochemistryMolecular BiologyBiocatalysisEnzymologyNucleic Acid BiochemistryCarbohydrate SynthesisGlycosidic Bond FormationNucleic Acid SynthesisNucleobase ChemistryGlycosyltransferase PathwaysGlycosyltransferase-mediated BiosynthesisNucleotide-sugar Donor SynthesisSugar Nucleosides
Sugar nucleotides made easy: The new reagent “ImIm”, which is formed in situ in water, is shown to activate nucleoside 5′-phosphates to their imidazolides, these can subsequently couple with sugar-1-phosphates; the whole procedure takes place in water. This truly simple method yields a crude product mixture that can be used directly as a source of donors for glycosyltransferase-mediated oligsaccharide synthesis. In the scheme, B stands for the nucleobases U, A, or G. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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Masato Noguchi, Tomonari Tanaka, Hidetoshi Gyakushi et al. · The Journal of Organic Chemistry · 2009 · 187 citations
Boopathy Ramakrishnan, Premal S. Shah, Pradman K. Qasba · Journal of Biological Chemistry · 2001 · 124 citations · Full text