Efficient and accelerated growth of multifunctional dendrimers using orthogonal thiol-ene and SN2 reactions

Chem Commun (Camb). 2014 Feb 25;50(16):1983-5. doi: 10.1039/c3cc46633g.

Abstract

An orthogonal coupling strategy was developed by combining thiol-ene and SN2 reactions, which was subsequently applied to the accelerated synthesis of multifunctional dendrimers using carbohydrate building blocks. In surface plasmon resonance (SPR) studies, the β-d-galactopyranoside-coated dendrimer exhibited nM binding affinity with the bacterial LecA lectin extracted from Pseudomonas aeruginosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesins, Bacterial / chemistry
  • Dendrimers / chemical synthesis*
  • Dendrimers / chemistry
  • Molecular Structure
  • Pseudomonas aeruginosa / chemistry
  • Sulfhydryl Compounds / chemistry*
  • Surface Plasmon Resonance

Substances

  • Adhesins, Bacterial
  • Dendrimers
  • LecA protein, bacteria
  • Sulfhydryl Compounds