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  4. Chiral Bis(oxazoline) Ligand-Supported Alkyl Aluminum Cations
 
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Chiral Bis(oxazoline) Ligand-Supported Alkyl Aluminum Cations

Journal
ChemCatChem
Journal Volume
14
Journal Issue
11
Date Issued
2022
Author(s)
Hsu C.-P
Liu C.-A
Wen C.-C
Liu Y.-H
Lin Y.-F
CHING-WEN CHIU  
DOI
10.1002/cctc.202101715
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127424627&doi=10.1002%2fcctc.202101715&partnerID=40&md5=b00fa6e5226c5951be2b9c2460b23aca
https://scholars.lib.ntu.edu.tw/handle/123456789/626228
Abstract
Alkyl aluminum cations have shown high Lewis acidity and capability of catalyzing challenging organic transformations, however, the related chiral catalyst is scarcely documented. Herein, we report the generation of a series of weakly solvated or Lewis base-stabilized alkyl aluminum cationic complexes bearing chiral bis(oxazoline) ligands. The increase of steric hindrances at the ligand backbone and the aluminum center were found to significantly increase the complex stability. In the Gutmann–Beckett experiment and fluoride ion affinity calculation, these complexes display Lewis acidity greater than B(C6F5)3 and the reported tetra-coordinate aluminum cation. Preliminary catalytic studies revealed that the aluminum cation catalysts can effectively promote hydroboration of ketone and hydrosilylation of un-activated olefin, despite only poor ee values were obtained. © 2022 Wiley-VCH GmbH.
Subjects
aluminum cation; bis(oxazoline) ligand; catalysis; Lewis acid; low-coordinate
Other Subjects
Aluminum compounds; Catalysts; Fluorine compounds; Ketones; Ligands; Positive ions; Aluminum cation; Bis(oxazoline) ligands; Cationic complexes; Chiral bis(oxazoline) ligands; Chiral catalyst; Lewis Acid; Lewis acidity; Lewis base; Low-coordinate; Organic transformations; Hydrosilylation
Type
journal article

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