Unnatural cyclopeptide synthesis via Cu-catalyzed 1,3-dipolar cycloaddition of azomethine ylides

Cyclic peptides are valued synthetic targets in organic and medicinal chemistry. Herein, we report an efficient strategy for the synthesis of unnatural cyclic peptides via the Cu-catalyzed 1,3-dipolar cycloaddition of azomethylene ylides. Linear precursors of different lengths and bearing diverse am...

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Detalles Bibliográficos
Autores: Gallent Ros, Enrique, Alonso Montero, María Inés, Carretero Gonzálvez, Juan Carlos, Rodríguez Garrido, Nuria, Adrio Sevilla, Francisco Javier
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/718779
Acceso en línea:http://hdl.handle.net/10486/718779
https://dx.doi.org/10.1021/acs.orglett.4c04036
Access Level:acceso abierto
Palabra clave:Adition reactions
azomethine
cyclization
peptides and proteins
precursors
Química
Descripción
Sumario:Cyclic peptides are valued synthetic targets in organic and medicinal chemistry. Herein, we report an efficient strategy for the synthesis of unnatural cyclic peptides via the Cu-catalyzed 1,3-dipolar cycloaddition of azomethylene ylides. Linear precursors of different lengths and bearing diverse amino acids (26 examples) are shown to be compatible with this method, affording good yields and complete endo-diastereoselectivities. Density functional theory (DFT) calculations support a stepwise mechanism in which Cu plays a key role in the preorganization of the reactants