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
- Yunpeng Ge
- Zeyuan Dong (ORCID: https://orcid.org/0000-0001-6509-9724)
- Ze Lin
- Chenhao Yao (ORCID: https://orcid.org/0009-0001-0159-2568)
- Jun Tian
- Siyuan Wang (ORCID: https://orcid.org/0000-0001-7293-1988)
- Changqing Zhang (ORCID: https://orcid.org/0000-0003-1410-6650)
- Lei Zhang (ORCID: https://orcid.org/0000-0003-4484-4347)
- Zhaocheng Xu
Institutions
- Jilin University (CN)
- Jilin Medical University (CN)
- Medicina (PL)
- Shenzhen Technology University (CN)
- State Key Laboratory of Supramolecular Structure and Materials
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
- National Natural Science Foundation of China
- Fundamental Research Funds for the Central Universities