» Articles » PMID: 17067955

A Review: Synthesis of Aryl C-glycosides Via the Heck Coupling Reaction

Overview
Specialty Biochemistry
Date 2006 Oct 28
PMID 17067955
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

In this article, we focus on the synthesis of aryl C-glycosides via Heck coupling. It is organized based on the type of structures used in the assembly of the C-glycosides (also called C-nucleosides) with the following subsections: pyrimidine C-nucleosides, purine C-nucleosides, and monocyclic, bicyclic, and tetracyclic C-nucleosides. The reagents and conditions used for conducting the Heck coupling reactions are discussed. The subsequent conversion of the Heck products to the corresponding target molecules and the application of the target molecules are also described.

Citing Articles

Cancer cell target discovery: comparing laboratory evolution of expanded DNA six-nucleotide alphabets with standard four-nucleotide alphabets.

Shaker S, Li J, Wan S, Xuan H, Long J, Cao H Nucleic Acids Res. 2025; 53(4).

PMID: 39950344 PMC: 11826092. DOI: 10.1093/nar/gkaf072.


Design and Synthesis of Small Molecule Probes of MDA-9/Syntenin.

Sankaranarayanan N, Villuri B, Nagarajan B, Lewicki S, Das S, Fisher P Biomolecules. 2024; 14(10).

PMID: 39456220 PMC: 11505911. DOI: 10.3390/biom14101287.


A selective and atom-economic rearrangement of uridine by cascade biocatalysis for production of pseudouridine.

Pfeiffer M, Ribar A, Nidetzky B Nat Commun. 2023; 14(1):2261.

PMID: 37081027 PMC: 10116470. DOI: 10.1038/s41467-023-37942-7.


Preparation and characterization of Pd supported on 5-carboxyoxindole functionalized cell@FeO nanoparticles as a novel magnetic catalyst for the Heck reaction.

Mohammadnia M, Poormirzaei N Nanoscale Adv. 2022; 3(7):1917-1926.

PMID: 36133091 PMC: 9419787. DOI: 10.1039/d0na00954g.


A new and informative [a,b,c,d] nomenclature for one-pot multistep transformations: a simple tool to measure synthetic efficiency.

Indu S, Kaliappan K RSC Adv. 2022; 8(38):21292-21305.

PMID: 35557999 PMC: 9088519. DOI: 10.1039/c8ra03338b.