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Updated: Apr 26, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
A hydrazide-anchored dendron scaffold for chemoselective ligation strategies
Liz O'Donovan1, Paul A De Bank
1Department of Pharmacy and Pharmacology and Centre for Regenerative Medicine, University of Bath, Bath, BA2 7AY, UK. p.debank@bath.ac.uk.
Abstract:
Chemoselective ligation, including "click" chemistry, has found wide utility in general synthetic strategies and the specific modification of polymers and biomolecules. This has resulted in a number of applications of such approaches, particularly in the biomedical area, including diagnostic imaging and drug delivery. However, tools to chemoselectively decorate target molecules with multiple copies of a particular drug, ligand or label are lacking. We describe the design and synthesis of a hydrazide-anchored dendron scaffold for chemoselective ligation to carbonyl moieties, and demonstrate its use in the modification of aldehyde-rich surfaces with the RGD integrin-binding ligand.

