Palladium-Mediated Arylation of Lysine in Unprotected Peptides

A mild method for the arylation of lysine in an unprotected peptide is presented. In the presence of a preformed biarylphosphine-supported palladium(II)-aryl complex and a weak base, lysine amino groups underwent C−N bond formation at room temperature. The process generally exhibited high selectivit...

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Bibliographic Details
Main Authors: Lee, Hong Geun (Contributor), Lautrette, Guillaume (Contributor), Pentelute, Bradley L. (Contributor), Buchwald, Stephen Leffler (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Chemistry (Contributor)
Format: Article
Language:English
Published: Wiley-Blackwell, 2018-05-02T18:50:17Z.
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