摘要
烯烃酰化反应被广泛用于制备结构丰富且高附加值的酮、醛、羧酸及其衍生物.多组分串联N-杂环卡宾催化和过渡金属催化的烯烃α-酰化反应具有高效、高选择性的优点,然而受限的反应模式和底物范围限制了反应的发展.光催化烯烃α-酰化反应突破了这一限制,具有更丰富、更广泛的底物适用范围.以研究策略为线索,对这一快速的研究进展进行了总结和展望.
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 viaα-acylation.Multicomponent tandemα-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 theα-acylation of olefins with broad substrate scope.The research progress and prospect for the future development in this active research field is highlighted.
作者
侯虹宇
程元元
陈彬
佟振合
吴骊珠
Hou Hongyu;Cheng Yuanyuan;Chen Bin;Tung Chenho;Wu Lizhu(Key Laboratory of Photochemical Conversion and Optoelectronic Materials,Technical Institute of Physics and Chemistry,Chinese Academy of Sciences,Beijing 100190;School of Future Technology,University of Chinese Academy of Sciences,Beijing 100049)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2023年第3期1012-1022,共11页
Chinese Journal of Organic Chemistry
基金
国家重点研发计划(Nos.2021YFA1500100,2022YFA1503200,2021YFA1500800)
国家自然科学基金(Nos.22193013,22088102,21933007)
中国科学院战略性先导科技专项(No.XDB17000000)
中国科学院前沿科学重点研究计划(No.QYZDY-SSWJSC029)资助项目
关键词
烯烃α-酰化
双官能团化
光催化
自由基级联
α-acylation of olefins
difunctionalization
photocatalysis
radical cascade