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Visible-Light Photoredox-Catalyzed Giese Reaction of α-Silyl Ethers with Various Michael Acceptors

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Abstract
We developed a photocatalyzed Giese reaction of various weakly activated Michael acceptors with a neutral silicon-based radical precursor and applied it at large-scale using a continuous flow reactor. The developed method successfully overcomes the substrate scope limitations of previous studies, shows good functional groups tolerance, and affords good to excellent yields. On the basis of mechanistic studies, we propose a reaction mechanism that involves an in situ generated alkoxymethyl radical via single-electron oxidation of α-trimethylsilyl-substituted ethers.
Issued Date
2023
Young Woo Kang
Ran Hui Kim
Shafrizal Rasyid Atriardi
Sang Kook Woo
Type
Article
Keyword
EthersEthyl groupsFourier transform infrared spectroscopyLiquidsOrganic compounds
DOI
10.1021/acs.joc.2c02754
URI
https://oak.ulsan.ac.kr/handle/2021.oak/17683
Publisher
JOURNAL OF ORGANIC CHEMISTRY
Language
영어
ISSN
0022-3263
Citation Volume
88
Citation Number
6
Citation Start Page
3555
Citation End Page
3566
Appears in Collections:
Natural Science > Chemistry
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