Alkali-Cation-Selective Arylation Promoted by Ion Recognition of Foldamers

To explore alkali-cation selectivity at the chemical reaction level, in this work, we for the first time focused on the different behaviors of potassium and sodium ions in intra- and intermolecular arylation. We prepared a series of aromatic foldamers based on pyridine/oxadiazole alternating sequences as the catalysts for the arylation. Our studies revealed that foldamers can selectively recognize K<sup>+</sup> over Na<sup>+</sup> and the interactions between foldamers and K<sup>+</sup> drive the arylation with a significant yield. In contrast, no trace of the product can be found with Na<sup>+</sup>. Furthermore, foldamers, with biased handedness, can afford products with optical activity. The balance between two enantiomers of products can be freely controlled by the different conformations of foldamers.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2024-12-24
DOI
https://doi.org/10.1021/acs.orglett.4c04055
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Alkali-Cation-Selective Arylation Promoted by Ion Recognition of Foldamers

Yunpeng Ge, Zeyuan Dong, Ze Lin, Chenhao Yao et al.
Organic Letters
Chemical Synthesis and Analysis
article

Alkali-Cation-Selective Arylation Promoted by Ion Recognition of Foldamers

Yunpeng Ge, Zeyuan Dong, Ze Lin, Chenhao Yao, Jun Tian, Siyuan Wang, Changqing Zhang, Lei Zhang, Zhaocheng Xu
article en

Abstract

To explore alkali-cation selectivity at the chemical reaction level, in this work, we for the first time focused on the different behaviors of potassium and sodium ions in intra- and intermolecular arylation. We prepared a series of aromatic foldamers based on pyridine/oxadiazole alternating sequences as the catalysts for the arylation. Our studies revealed that foldamers can selectively recognize K<sup>+</sup> over Na<sup>+</sup> and the interactions between foldamers and K<sup>+</sup> drive the arylation with a significant yield. In contrast, no trace of the product can be found with Na<sup>+</sup>. Furthermore, foldamers, with biased handedness, can afford products with optical activity. The balance between two enantiomers of products can be freely controlled by the different conformations of foldamers.

Organic LettersVol. 27(1)
Jilin University (CN), Jilin Medical University (CN), Medicina (PL), Shenzhen Technology University (CN), State Key Laboratory of Supramolecular Structure and Materials
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 79%
Chemical Synthesis and Analysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.