2018
DOI: 10.3762/bjoc.14.95
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Synthetic avenues towards a tetrasaccharide related to Streptococcus pneumonia of serotype 6A

Abstract: Streptococcus pneumonia (SPn) is a Gram-positive bacterium which causes life threatening diseases. The bacteria protect themselves against non-specific host defence by an external polysaccharide (PS) capsule which bears a repeating unit, α-D-Galp(1->3)-α-D-Glcp(1->3)-α-L-Rhap(1->3)-D-Rib (SPn 6A). A closer look at the structure reveals the presence of α-linked galactose and glucose residues. The synthesis of these 1,2-cis glycosidic linkages are considered challenging particularly in the context of a one-pot o… Show more

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Cited by 8 publications
(5 citation statements)
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“…2B) 41 . Serotype 6 A' CPS, based on tetrasaccharides, includes a rhamnose modification 42 . Streptococcus suis (S. suis) strains were initially classified into 35 serotypes based on CPS antigenicity [43][44][45] , later revised to 33 serotypes 46 .…”
Section: Serotypes and Pathogenicitymentioning
confidence: 99%
“…2B) 41 . Serotype 6 A' CPS, based on tetrasaccharides, includes a rhamnose modification 42 . Streptococcus suis (S. suis) strains were initially classified into 35 serotypes based on CPS antigenicity [43][44][45] , later revised to 33 serotypes 46 .…”
Section: Serotypes and Pathogenicitymentioning
confidence: 99%
“…Hence, the orthogonal glycosylation between donor 17 and acceptor 18 62 in the presence of tert-butyldimethylsilyl trifluorosulfonate Given that only a modest selectivity of α/β = 6:1 and lower yields were observed for the synthesis of disaccharide 6 and the surprising outcome of only α/β = 1:4 for a β-selective glycosylation to obtain trisaccharide 20 as an inseparable mixture (Scheme 1), we explored different donors. One of the best reactions turned out to be the coupling between donor 26 65 and acceptor 18 using NIS/TMSOTf to obtain 27 in 71% with lower selectivity (α/β = 2:1) than obtained for disaccharide 6 as an inseparable mixture (Scheme 2). The anomers were separated after the benzylidene cleavage to afford 4,6-diol 28 in 53%.…”
Section: Synthetic Strategymentioning
confidence: 99%
“…In continuation of this program, we describe here the preparation of similar pseudotetrasaccharide 2 that represents the repeating unit of the type 6A CP. Although several oligosaccharides related to the type 6A CP have been synthesized ( Slaghek et al, 1991 ; Parameswar et al, 2007 ; Parameswar et al, 2008 ; Parameswar et al, 2009 ; Chaudhury et al, 2018 ), none of them contained both the phosphate bridge and a spacer group that enables further conjugation with labels or protein carriers.…”
Section: Introductionmentioning
confidence: 99%