“One-pot” protection, glycosylation, and protection–glycosylation strategies of carbohydrates

SS Kulkarni, CC Wang, NM Sabbavarapu… - Chemical …, 2018 - ACS Publications
Carbohydrates, which are ubiquitously distributed throughout the three domains of life, play
significant roles in a variety of vital biological processes. Access to unique and …

Chemical O‐Glycosylations: An Overview

R Das, B Mukhopadhyay - ChemistryOpen, 2016 - Wiley Online Library
The development of glycobiology relies on the sources of particular oligosaccharides in their
purest forms. As the isolation of the oligosaccharide structures from natural sources is not a …

Recent advances in chemical synthesis of polysaccharides

Y Wu, XS Ye - Acta Chimica Sinica, 2019 - sioc-journal.cn
Polysaccharides are a class of bio-macromolecules with highly complex structures that are
widely found in living organisms such as microorganisms, plants and animals …

One‐pot methods for the protection and assembly of sugars

MML Zulueta, D Janreddy… - Israel Journal of Chemistry, 2015 - Wiley Online Library
In recent years, there has been rapid expansion of glycan synthesis, fueled by the
recognition that the structural complexity of sugars translates to a myriad of biological …

One-pot glycosylation strategy for rapid access of oligosaccharides with wide range of molecular diversity

R Sangwan, PK Mandala - Current Organic Chemistry, 2021 - benthamdirect.com
In carbohydrate chemistry, the synthesis of complex saccharides with well-defined structures
is the most formidable process as it is quite strenuous to isolate carbohydrates in acceptable …

Use of iodine for efficient and chemoselective glycosylation with glycosyl ortho-alkynylbenzoates as donor in presence of thioglycosides

S Dutta, S Sarkar, SJ Gupta, AK Sen - Tetrahedron Letters, 2013 - Elsevier
A novel and high yielding glycosylation protocol with glycosyl ortho-alkynylbenzoates as
donors and iodine as promoter is described. The donors are stable and can be …

One-pot iterative glycosylations toward a tetrasaccharide related to the O-specific polysaccharide from Escherichia coli O132

VN Mishra, PK Mandal - Journal of Carbohydrate Chemistry, 2021 - Taylor & Francis
An efficient synthetic strategy has been developed for the synthesis of a tetrasaccharide
related to the O-specific polysaccharide from Escherichia coli O132 as their 2-aminoethyl …

Synthesis of tri-, penta-, and heptasaccharides, functionalized with orthogonally N-protected amino residues at the reducing and non-reducing ends

T Fyrner, SCT Svensson, P Konradsson - Tetrahedron, 2012 - Elsevier
The synthesis of four bifunctionalized orthogonally N-protected oligosaccharides derived
from lactose and mannose, intended as cross-linking derivatives, is described. The …

Convergent Synthesis of the Pentasaccharide Repeating Unit of the O-Antigen of Escherichia coli O36

PK Mandal - Synthesis, 2015 - thieme-connect.com
An efficient synthesis of the pentasaccharide repeating unit of the O-antigen of Escherichia
coli O36 is reported. A stereoselective [2+ 3] block glycosylation method has been exploited …

STRATEGIES FOR ONE‐POT SYNTHESIS OF OLIGOSACCHARIDES

B Yang, K Yoshida, X Huang - … Synthesis: Strategies and …, 2016 - Wiley Online Library
One‐pot oligosaccharide synthesis refers to approaches by which one glycosyl building
block is subjected to successive chemical reactions in the same flask without the need to …