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Detalle de: A Late-Stage Synthetic Approach to Lanthionine-Containing Peptides via S-Alkylation on Cyclic Sulfamidates Promoted by Molecular Sieves

Title A Late-Stage Synthetic Approach to Lanthionine-Containing Peptides via S-Alkylation on Cyclic Sulfamidates Promoted by Molecular Sieves
Abstract

A one-pot, high-yield procedure for synthesizing lanthionine-containing peptides was developed. It relies on the S-alkylation of cysteine-containing peptides with chiral cyclic sulfamidates. The key feature of this approach is the use of mild reaction conditions (only activated molecular sieves are employed as the catalyst), leading to good chemoselectivity and excellent stereochemical control. The potential of the new methodology has been investigated by synthesizing the thioether ring of a natural lantibiotic, Haloduracin β.

Apa Reference De Luca, S., Digilio, G., Verdoliva, V., Saviano, M., Menchise, V., Tovillas, P., Jiménez-Osés, G. & Peregrina, J.M. (2018). A Late-Stage Synthetic Approach to Lanthionine-Containing Peptides via S-Alkylation on Cyclic Sulfamidates Promoted by Molecular Sieves. Organic Letters, 20(23), 7478-7482. 10.1021/acs.orglett.8b03254
Doi 10.1021/acs.orglett.8b03254
Publication Date 14 Nov 2018
Publication Type Article
Researcher Gonzalo Jiménez-Osés
Ontology
Research Groups
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