Peptide macrocyclization by transition metal catalysis

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. © The Royal Society of Chemistry.

Rivera D.G.1, 2 , Ojeda-Carralero G.M.1, 2 , Reguera L.2 , Van Der Eycken E.V.
Royal Society of Chemistry
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  • 1 Laboratory for Organic and Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, Leuven, B-3001, Belgium
  • 2 Center for Natural Product Research, Faculty of Chemistry, University of Havana, Zapata y G, Havana, 10400, Cuba
  • 3 Peoples' Friendship University of Russia, RUDN University, Miklukho-Maklaya Street 6, Moscow, 117198, Russian Federation
Ключевые слова
Activation analysis; Biology; Copper compounds; Covalent bonds; Cycloaddition; Hydrocarbons; Peptides; Sulfur compounds; Transition metals; Conformational constraints; Derivatization method; Diversity generations; Future perspectives; Palladium-catalyzed cross-couplings; Peptide sequences; Ring closing metathesis; Transition metal catalysis; Catalysis
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