Issue 23, 2014

A mild and selective Pd-mediated methodology for the synthesis of highly fluorescent 2-arylated tryptophans and tryptophan-containing peptides: a catalytic role for Pd0 nanoparticles?

Abstract

A Pd-mediated direct C–H bond functionalisation of tryptophan has been developed, both as a single amino acid residue and within peptides. Important mechanistic insight into this process has been gained by characterising a Pd catalytically competent nanoparticle phase which evolves during the early stages of reaction.

Graphical abstract: A mild and selective Pd-mediated methodology for the synthesis of highly fluorescent 2-arylated tryptophans and tryptophan-containing peptides: a catalytic role for Pd0 nanoparticles?

Supplementary files

Article information

Article type
Communication
Submitted
06 Nov 2013
Accepted
25 Jan 2014
First published
10 Feb 2014
This article is Open Access
Creative Commons BY license

Chem. Commun., 2014,50, 3052-3054

Author version available

A mild and selective Pd-mediated methodology for the synthesis of highly fluorescent 2-arylated tryptophans and tryptophan-containing peptides: a catalytic role for Pd0 nanoparticles?

T. J. Williams, A. J. Reay, A. C. Whitwood and I. J. S. Fairlamb, Chem. Commun., 2014, 50, 3052 DOI: 10.1039/C3CC48481E

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