Literature DB >> 35048443

Pedal to the Metal: The Homogeneous Catalysis of the Native Chemical Ligation Reaction.

Vincent Diemer1, Olga Firstova1, Vangelis Agouridas1,2, Oleg Melnyk1.   

Abstract

The native chemical ligation reaction of peptide thioesters with cysteinyl peptides is a pivotal chemical process in the production of native or modified peptides and proteins, and well beyond in the preparation of various biomolecule analogs and materials. To benefit from this reaction at its fullest and to access all the possible applications, the experimentalist needs to know the factors affecting its rate and how to control it. This concept article presents the fundamental principles underlying the rate of the native chemical ligation and its homogeneous catalysis by nucleophiles. It has been prepared to serve as a quick guide in the search for an appropriate catalyst.
© 2022 Wiley-VCH GmbH.

Entities:  

Keywords:  chemoselectivity; desulfurization; homogeneous catalysis; native chemical ligation; nucleophilic catalysis; thiol-thioester exchange

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Year:  2022        PMID: 35048443     DOI: 10.1002/chem.202104229

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Redox-Controlled Chemical Protein Synthesis: Sundry Shades of Latency.

Authors:  Vangelis Agouridas; Nathalie Ollivier; Jérôme Vicogne; Vincent Diemer; Oleg Melnyk
Journal:  Acc Chem Res       Date:  2022-09-09       Impact factor: 24.466

2.  Thioester deprotection using a biomimetic NCL approach.

Authors:  Valentina Villamil; Cecilia Saiz; Graciela Mahler
Journal:  Front Chem       Date:  2022-08-22       Impact factor: 5.545

3.  Controlled Selectivity through Reversible Inhibition of the Catalyst: Stereodivergent Semihydrogenation of Alkynes.

Authors:  Jie Luo; Yaoyu Liang; Michael Montag; Yael Diskin-Posner; Liat Avram; David Milstein
Journal:  J Am Chem Soc       Date:  2022-07-15       Impact factor: 16.383

  3 in total

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