Published in

Royal Society of Chemistry, Organic and Biomolecular Chemistry, 32(18), p. 6265-6275, 2020

DOI: 10.1039/d0ob01061h

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Selective modification of sulfamidate-containing peptides

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Hybrid peptides whose N-terminal residues are activated in the form of α-methylisoserine cyclic sulfamidates exhibit rich reactivity as electrophiles, allowing site- and stereoselective modifications at different backbone and side chain positions.