碘化钠-三苯基膦介导的光氧化还原醛亚胺烷基化
收稿日期: 2021-02-22
修回日期: 2021-04-02
网络出版日期: 2021-04-29
基金资助
国家自然科学基金(21662022); Ronald J. Quinn AM院士工作站和云南省教育厅高校创新团队(2019IC003)
Sodium Iodide-Triphenylphosphine-Mediated Photoredox Alkylation of Aldimines
Received date: 2021-02-22
Revised date: 2021-04-02
Online published: 2021-04-29
Supported by
National Natural Science Foundation of China(21662022); Ronald J Quinn AM Academician Workstation and the Program for Innovative Research Team (in Science and Technology) in Universities of Yunnan Province(2019IC003)
邵子宴 , 周庆丽 , 王建成 , 汤芮 , 沈悦海 . 碘化钠-三苯基膦介导的光氧化还原醛亚胺烷基化[J]. 有机化学, 2021 , 41(7) : 2676 -2683 . DOI: 10.6023/cjoc202102039
The photoredox reactions involving electron donor-acceptor (EDA) complexes have attracted significant attentions in the last decade. Very recently, the sodium iodide-triphenylphosphine-N-acyloxyphthalimide EDA complex has been discovered and employed in developing several net redox-neutral photoreactions. Herein, the EDA complex has been applied in a net reductive setup for the first time to establish a photoredox alkylation of aldimines without photosensitizer. The reaction affords not only high yields for secondary, tertiary andα-heterosubstituted alkyl radicals, but also high yields for primary alkyl radicals, and moderate to high yields for electron-rich or secondary benzylic radicals, two difficult groups of radicals in previous studies. This work provides an efficient and reliable approach for the synthesis of unnatural amino acids and amines.
Key words: photoredox; aldimine; electron donor-acceptor complex
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