Surface Glycans of Candida albicans and Other Pathogenic Fungi: Physiological Roles, Clinical Uses, and Experimental Challenges

J Masuoka - Clinical microbiology reviews, 2004 - journals.asm.org
Although fungi have always been with us as commensals and pathogens, fungal infections
have been increasing in frequency over the past few decades. There is a growing body of …

Progress and challenges in the synthesis of sequence controlled polysaccharides

G Fittolani, T Tyrikos-Ergas, D Vargová… - Beilstein Journal of …, 2021 - beilstein-journals.org
The sequence, length and substitution of a polysaccharide influence its physical and
biological properties. Thus, sequence controlled polysaccharides are important targets to …

Electrochemical generation of glycosyl triflate pools

T Nokami, A Shibuya, H Tsuyama, S Suga… - Journal of the …, 2007 - ACS Publications
Glycosyl triflates, which serve as important intermediates in glycosylation reactions, were
generated and accumulated by the low-temperature electrochemical oxidation of …

Mimicry of an HIV broadly neutralizing antibody epitope with a synthetic glycopeptide

SM Alam, B Aussedat, Y Vohra, RR Meyerhoff… - Science translational …, 2017 - science.org
A goal for an HIV-1 vaccine is to overcome virus variability by inducing broadly neutralizing
antibodies (bnAbs). One key target of bnAbs is the glycan-polypeptide at the base of the …

Automated solution-phase synthesis of β-1, 4-mannuronate and β-1, 4-mannan

SL Tang, NLB Pohl - Organic letters, 2015 - ACS Publications
The first automated solution-phase synthesis of β-1, 4-mannuronate and β-1, 4-mannan
oligomers has been accomplished by using a β-directing C-5 carboxylate strategy. By …

Is an acyl group at O-3 in glucosyl donors able to control α-stereoselectivity of glycosylation? The role of conformational mobility and the protecting group at O-6

BS Komarova, MV Orekhova, YE Tsvetkov… - Carbohydrate …, 2014 - Elsevier
The stereodirecting effect of a 3-O-acetyl protecting group, which is potentially capable of the
remote anchimeric participation, and other protecting groups in 2-O-benzyl glucosyl donors …

Pre‐activation‐based one‐pot synthesis of an α‐(2, 3)‐sialylated core‐fucosylated complex type bi‐antennary N‐glycan dodecasaccharide

B Sun, B Srinivasan, X Huang - Chemistry–A European …, 2008 - Wiley Online Library
Synthesis of N‐glycans is of high current interests due to their important biological
properties. A highly efficient convergent strategy based on the pre‐activation method for …

Glycosylation with sulfoxide-based glycosyl donors

P Wu, J Zeng, L Meng, Q Wan - Chemical Communications, 2024 - pubs.rsc.org
Sulfoxides have emerged as pivotal constituents in modern carbohydrate chemistry. As
anomeric leaving groups, sulfinyl moieties may occupy positions directly at the anomeric …

Benzylidene Acetal Fragmentation Route to 6-Deoxy Sugars:  Direct Reductive Cleavage in the Presence of Ether Protecting Groups, Permitting the Efficient, Highly Stereocontrolled Synthesis of β-d-Rhamnosides from d-Mannosyl Glycosyl Donors …

D Crich, Q Yao - Journal of the American Chemical Society, 2004 - ACS Publications
An approach to the stereocontrolled synthesis of β-d-rhamnopyranosides is described in
which 2, 3-O-benzyl or related 4, 6-O-[α-(2-(2-iodophenyl) ethylthiocarbonyl) benzylidene] …

Arabinofuranosides from mycobacteria: synthesis of a highly branched hexasaccharide and related fragments containing β-arabinofuranosyl residues

H Yin, FW D'Souz, TL Lowary - The Journal of organic chemistry, 2002 - ACS Publications
The synthesis of 11 oligosaccharides (4− 14) containing β-arabinofuranosyl residues is
reported. The glycans are all fragments of two polysaccharides, arabinogalactan and …