Recent advances on the one-pot synthesis to assemble size-controlled glycans and glycoconjugates and polysaccharides.

Carbohydr Polym

School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, Wenyuan Road 1, Nanjing 210023, China. Electronic address:

Published: April 2021

AI Article Synopsis

  • Glycans and glycoconjugates are essential macromolecules found in all living organisms, playing crucial roles in various biological functions like immune response, inflammation, and cell signaling.
  • The complexity and diversity of these molecules make it challenging to fully understand their functions and potential applications, particularly in drug development.
  • Recent advancements in controlled one-pot synthesis methods allow for the production of more uniform oligosaccharides and polysaccharides, which could enhance the creation of carbohydrate-based therapeutics.

Article Abstract

Glycans and glycoconjugates in nature include macromolecules with important biological activities and widely distributed in all living organisms. These oligosaccharides and polysaccharides play important roles in a variety of normal physiological and pathological processes, such as cell metastasis, signal transduction, intercellular adhesion, inflammation, and immune response. However, the heterogeneity of naturally occurring glycans and glycoconjugates complicates detailed structure-activity relationship studies resulting in an incomplete understanding of their mechanisms of action and hindering further applications. Therefore, the synthesis of homogeneous, or nearly homogeneous, structurally defined glycans is of great significance for the development of carbohydrate-based drugs. One-pot synthesis represents the fastest strategy to assemble oligosaccharides and polysaccharides, although unfortunately, typically relies on random assembly. In this review, we examine the progress that has been made in the controlled one-pot synthesis of homogeneous or nearly homogeneous oligosaccharides and polysaccharides providing a broad spectrum of options to access size-controlled glycan products.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.carbpol.2021.117672DOI Listing

Publication Analysis

Top Keywords

one-pot synthesis
12
glycans glycoconjugates
12
oligosaccharides polysaccharides
12
synthesis homogeneous
8
homogeneous homogeneous
8
advances one-pot
4
synthesis
4
synthesis assemble
4
assemble size-controlled
4
glycans
4

Similar Publications

A one-pot, acid-, base-, and metal-free, multicomponent strategy has been developed to synthesize spiro thiochromene-oxindole derivatives as potential anti-inflammatory agents. The synthesized compounds were screened for their anti-inflammatory activity by inhibiting heat-induced Bovine Serum Albumin (BSA) denaturation assay, revealing moderate to good efficacy. Compounds 4e, 4k, and 4h exhibited the highest activity, inhibiting BSA denaturation by 90.

View Article and Find Full Text PDF

Potassium Persulfate Promoted the One-Pot and Selective -Functionalization of Pyrazoles under Acidic Conditions.

ACS Omega

December 2024

SupraSelen Laboratory, Department of Chemistry, Universidade Federal Fluminense, Institute of Chemistry, Campus do Valonguinho, 24020-141 Niterói-RJ, Brazil.

Our research presents selective direct selenylation at the C-4 pyrazole ring using KSO as an oxidant under simple and mild conditions. This elegant synthesis involves the one-pot method under acidic conditions, thus minimizing reaction steps and waste generation. This innovative method allowed us to create a library of 4-selanylpyrazoles in good to excellent yields.

View Article and Find Full Text PDF

Photocatalytic → isomerization of -bromofluoroalkenes: stereoselective synthesis of β-fluorostyrene derivatives.

Org Biomol Chem

January 2025

Department of Applied Chemistry, Faculty of Fundamental Engineering, Nippon Institute of Technology, 4-1 Gakuendai, Miyashiro-machi, Minamisaitama-gun, Saitama 345-8501, Japan.

Stereoselective synthesis of β-fluorostyrene derivatives has been achieved. Selective isomerization of -bromofluoroalkenyl benzenes bearing various -substituents is enabled by using Ir photocatalysts with high triplet energy. Subsequent one-pot transition-metal (TM)-catalyzed reactions enable pot-economical synthesis of monofluoroalkenes in a stereoselective manner.

View Article and Find Full Text PDF

Introduction: An efficient and four-component one-pot facile synthesis of tetra-substituted imidazole is achieved by cyclo-condensation reaction of benzil with subsequent successive substitution of aromatic aldehydes, ester substituted amine and ammonium acetate via refluxing the mixture for almost two hours at 140°C.

Method: The ending point of the understudy reaction was examined by TLC after regular intervals. Synthesized 1,2,4-tetrasubstituted imidazoles were characterized by physical data and the structural features were analyzed using spectroscopic techniques such as FTIR, NMR and elemental analysis.

View Article and Find Full Text PDF

A simple synthetic method for pinocembrin from cinnamic acid and 1,3,5-trihydroxybenzene was provided. This method can be performed in one-pot two steps reaction using inexpensive chemical reagents, whereas conventional methods need multiple steps from somewhat expensive starting reagents. The experimental procedure is facilitated, that is, to a DMF solution of cinnamoyl chloride generated in situ, a solution of 1,3,5-trihydroxybenzene and AlCl in DCE/PhNO was added, and the resultant mixture was heated to afford pinocembrin.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!