Synthesis of water-soluble hypervalent iodine reagents for fluoroalkylation of biological thiols?
Organic & Biomolecular Chemistry Pub Date: 2019-11-13 DOI: 10.1039/C9OB02115A
Abstract
New open-chain and water-soluble hypervalent iodine reagents were synthesized and used for the transfer of fluoroalkyl groups to sulfur atoms of cysteine and cysteine-containing peptides under biocompatible conditions. Some of the reagents displayed excellent reactivity despite their limited stability in aqueous media. In reactions with a short cysteine-containing peptide, in addition to the expected S-fluoroalkylated product, a range of side-products were obtained. The amount of side-products depended on the conditions used (type of reagent, concentration, and pH). With highly activated hypervalent iodine reagents, a new reactive mode was observed – reaction with disulfides to form fluoroalkyl thiols.
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Journal Name:Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4