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Issue 7, 2020
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Peptide macrocyclization by transition metal catalysis

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Peptide macrocyclization has traditionally relied on lactam, lactone and disulfide bond-forming reactions that aim at introducing conformational constraints into small peptide sequences. With the advent of ruthenium-catalyzed ring-closing metathesis and copper-catalyzed alkyne–azide cycloaddition, peptide chemists embraced transition metal catalysis as a powerful macrocyclization tool with relevant applications in chemical biological and peptide drug discovery. This article provides a comprehensive overview of the reactivity and methodological diversification of metal-catalyzed peptide macrocyclization as a special class of late-stage peptide derivatization method. We report the evolution from classic palladium-catalyzed cross-coupling approaches to more modern oxidative versions based on C–H activation, heteroatom alkylation/arylation and annulation processes, in which aspects such as chemoselectivity and diversity generation at the ring-closing moiety became dominant over the last years. The transit from early cycloadditions and alkyne couplings as ring-closing steps to very recent 3d metal-catalyzed macrocyclization methods is highlighted. Similarly, the new trends in decarboxylative radical macrocyclizations and the interplay between photoredox and transition metal catalysis are included. This review charts future perspectives in the field hoping to encourage further progress and applications, while bringing attention to the countless possibilities available by diversifying not only the metal, but also the reactivity modes and tactics to bring peptide functional groups together and produce structurally diverse macrocycles.

Graphical abstract: Peptide macrocyclization by transition metal catalysis

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Article information

05 Nov 2019
First published
06 Mar 2020

Chem. Soc. Rev., 2020,49, 2039-2059
Article type
Review Article

Peptide macrocyclization by transition metal catalysis

D. G. Rivera, G. M. Ojeda-Carralero, L. Reguera and E. V. Van der Eycken, Chem. Soc. Rev., 2020, 49, 2039
DOI: 10.1039/C9CS00366E

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