光催化烯烃α-酰化反应
收稿日期: 2022-11-30
修回日期: 2023-01-13
网络出版日期: 2023-01-18
基金资助
国家重点研发计划(2021YFA1500100); 国家重点研发计划(2022YFA1503200); 国家重点研发计划(2021YFA1500800); 国家自然科学基金(22193013); 国家自然科学基金(22088102); 国家自然科学基金(21933007); 中国科学院战略性先导科技专项(XDB17000000); 中国科学院前沿科学重点研究计划(QYZDY-SSWJSC029)
α-Acylation of Olefins via Photocatalysis
Received date: 2022-11-30
Revised date: 2023-01-13
Online published: 2023-01-18
Supported by
National Key Research and Development Program of China(2021YFA1500100); National Key Research and Development Program of China(2022YFA1503200); National Key Research and Development Program of China(2021YFA1500800); National Natural Science Foundation of China(22193013); National Natural Science Foundation of China(22088102); National Natural Science Foundation of China(21933007); Strategic Priority Research Program of the Chinese Academy of Science(XDB17000000); Key Research Program of Frontier Sciences of the Chinese Academy of Science(QYZDY-SSWJSC029)
侯虹宇 , 程元元 , 陈彬 , 佟振合 , 吴骊珠 . 光催化烯烃α-酰化反应[J]. 有机化学, 2023 , 43(3) : 1012 -1022 . DOI: 10.6023/cjoc202211048
The cheap and readily available olefin substrates have received much attention for the synthesis of structurally rich and high value-added ketones, aldehydes, carboxylic acids and their derivatives via α-acylation. Multicomponent tandem α-acylation of olefins achieves high efficiency and selectivity by N-heterocyclic carbene or transition metal catalysis, albeit with narrow reaction modes and substrates. Rapid growth of photocatalysis in organic transformation has introduced new methodologies to undergo the α-acylation of olefins with broad substrate scope. The research progress and prospect for the future development in this active research field is highlighted.
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