Diastereoselective Anomeric C(sp<sup>3</sup>)−H Cyclization Towards the Design of New Cyclophane‐Braced Glycopeptides

Abstract Here we report a macrocyclization route towards the synthesis of glycophane peptides by a selective C−H arylation of the anomeric bond. This approach demonstrates the power of Pd‐catalysis C−H activation to access unusual cyclic peptides.

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Publication Details

Journal
Angewandte Chemie
Published
2024-11-08
DOI
https://doi.org/10.1002/ange.202418057
Citations
1
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
Field-Weighted Citation Impact
0.25
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article

Diastereoselective Anomeric C(sp3)−H Cyclization Towards the Design of New Cyclophane‐Braced Glycopeptides

Sakna Bazzi, Mehdi A. Beniddir, Juba Ghouilem, Vincent Gandon et al.
1 citations
Angewandte Chemie
Carbohydrate Chemistry and Synthesis
0.25
article

Diastereoselective Anomeric C(sp3)−H Cyclization Towards the Design of New Cyclophane‐Braced Glycopeptides

Sakna Bazzi, Mehdi A. Beniddir, Juba Ghouilem, Vincent Gandon, Dmytro Ryzhakov, Samir Messaoudi, Ameni Hadj Mohamed
article en
1 citations

Abstract

Abstract Here we report a macrocyclization route towards the synthesis of glycophane peptides by a selective C−H arylation of the anomeric bond. This approach demonstrates the power of Pd‐catalysis C−H activation to access unusual cyclic peptides.

Angewandte ChemieVol. 137(6)
Centre National de la Recherche Scientifique (FR), École Polytechnique (FR), École Nationale Supérieure de Techniques Avancées (FR), Université Paris-Saclay (FR), Laboratoire de Synthèse Organique (FR), Institut de Chimie Moléculaire et des Matériaux d'Orsay (FR)
Openalex Percentile: Top 47%
Carbohydrate Chemistry and Synthesis
0.25
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Diastereoselective Anomeric C(sp<sup>3</sup>)−H Cyclization Towards the Design of New Cyclophane‐Braced Glycopeptides — Sakna Bazzi, Mehdi A. Beniddir, et al. · Angewandte Chemie (2024) | TGRS Research Map | TGRS