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Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions

A novel conjugate addition/ring expansion (CARE) cascade reaction sequence is reported that enables medium-sized ring and macrocyclic bis-lactams to be prepared from primary amines and cyclic imides. The reactions are simple to perform, generally high yielding, and very broad in scope, especially wi...

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Detalles Bibliográficos
Autores principales: Palate, Kleopas Y., Yang, Zhongzhen, Whitwood, Adrian C., Unsworth, William P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905531/
https://www.ncbi.nlm.nih.gov/pubmed/35359493
http://dx.doi.org/10.1039/d1cb00245g
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author Palate, Kleopas Y.
Yang, Zhongzhen
Whitwood, Adrian C.
Unsworth, William P.
author_facet Palate, Kleopas Y.
Yang, Zhongzhen
Whitwood, Adrian C.
Unsworth, William P.
author_sort Palate, Kleopas Y.
collection PubMed
description A novel conjugate addition/ring expansion (CARE) cascade reaction sequence is reported that enables medium-sized ring and macrocyclic bis-lactams to be prepared from primary amines and cyclic imides. The reactions are simple to perform, generally high yielding, and very broad in scope, especially with respect to the primary amine component. CARE reactions can also be performed iteratively, enabling β-peptoid-based macrocyclic peptide mimetics to be ‘grown’ via well controlled, sequential 4-atom ring expansion reactions, with the incorporation of varied functionalised amines during each iteration.
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spelling pubmed-89055312022-03-30 Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions Palate, Kleopas Y. Yang, Zhongzhen Whitwood, Adrian C. Unsworth, William P. RSC Chem Biol Chemistry A novel conjugate addition/ring expansion (CARE) cascade reaction sequence is reported that enables medium-sized ring and macrocyclic bis-lactams to be prepared from primary amines and cyclic imides. The reactions are simple to perform, generally high yielding, and very broad in scope, especially with respect to the primary amine component. CARE reactions can also be performed iteratively, enabling β-peptoid-based macrocyclic peptide mimetics to be ‘grown’ via well controlled, sequential 4-atom ring expansion reactions, with the incorporation of varied functionalised amines during each iteration. RSC 2022-02-09 /pmc/articles/PMC8905531/ /pubmed/35359493 http://dx.doi.org/10.1039/d1cb00245g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Palate, Kleopas Y.
Yang, Zhongzhen
Whitwood, Adrian C.
Unsworth, William P.
Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
title Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
title_full Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
title_fullStr Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
title_full_unstemmed Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
title_short Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
title_sort synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905531/
https://www.ncbi.nlm.nih.gov/pubmed/35359493
http://dx.doi.org/10.1039/d1cb00245g
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