转鼓
化学
磷化氢
氨基酸
光催化
异氰
组合化学
氘
有机化学
催化作用
生物化学
量子力学
物理
亲核细胞
作者
Chunhua Ma,Xiaofeng Li,Xiya Chen,Xing He,Shuting Zhang,Yuqin Jiang,Bing Yu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-10-30
卷期号:25 (44): 8016-8021
被引量:29
标识
DOI:10.1021/acs.orglett.3c03193
摘要
Direct, economical, and green synthesis of deuterated α-amino phosphine oxides remains an elusive challenge in synthetic chemistry. Herein, we report a visible-light-driven umpolung strategy for synthesizing deuterated α-amino phosphine oxides from isocyanide using 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene as the photocatalyst and D2O as the deuterium source. Moreover, the streamlined and sustainable methodology can be applied in the modification of amino acids, natural products, and drugs. The strong antiproliferative activity of the desired products indicates that the method could provide a novel privileged scaffold for antitumor drug development.
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