Literature DB >> 1591756

Synthesis of nigero-oligosaccharides.

K Takeo1, S Kitamura, Y Murata.   

Abstract

Nigerose [alpha-D-Glcp-(1----3)-D-Glcp], nigerotriose, nigerotetraose, and nigeropentaose have been synthesized by chain elongation starting at the reducing end, from the corresponding octa-, undeca-, tetradeca-, and heptadeca-beta-D-acetates, respectively, via thioglycoside-mediated 1,2-cis coupling, using 1,2,4,6-tetra-O-acetyl-beta-D-glucopyranose as the glucosyl acceptor and methyl 2,3,4,6-tetra-O-benzyl-1-thio-beta-D-glucopyranoside, methyl 3-O-allyl-2,4,6-tri-O-benzyl-1-thio-beta-D-glucopyranoside, and methyl O-(2,3,4,6-tetra-O-benzyl-alpha-D-glucopyranosyl)-(1----3)-2,4,6-tri-O- benzyl-1-thio-beta-D-glucopyranoside as the donors.

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Year:  1992        PMID: 1591756     DOI: 10.1016/0008-6215(92)84098-d

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  1 in total

1.  Anomeric reactivity-based one-pot synthesis of heparin-like oligosaccharides.

Authors:  Tülay Polat; Chi-Huey Wong
Journal:  J Am Chem Soc       Date:  2007-10-03       Impact factor: 15.419

  1 in total

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