Issue 3, 2022

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

Abstract

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.

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

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Article information

Article type
Paper
Submitted
17 Dec. 2021
Accepted
08 Febr. 2022
First published
09 Febr. 2022
This article is Open Access
Creative Commons BY-NC license

RSC Chem. Biol., 2022,3, 334-340

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

K. Y. Palate, Z. Yang, A. C. Whitwood and W. P. Unsworth, RSC Chem. Biol., 2022, 3, 334 DOI: 10.1039/D1CB00245G

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