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Updated: Nov 23, 2025

Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation
Published on: August 1, 2018
Rapid access to Asp/Glu sidechain hydrazides as thioester precursors for peptide cyclization and glycosylation
Natalie G Barnes1, Kudakwashe Nyandoro1, Hanzhang Jin1
1Department of Chemistry, University College London, 20 Gordon Street, London, WC1H0AJ, UK. d.macmillan@ucl.ac.uk.
Abstract:
Head-to-sidechain macrocylic peptides, and neoglycopeptides, were readily prepared by site-specific amidation of aspartic and glutamic acid sidechain hydrazides. Hydrazides, serving as latent thioesters, were introduced through regioselective opening of the corresponding Nα-Fmoc protected anhydride precursors.
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