Department of Chemistry, College of Chemistry and Chemical Engineering, and Key Laboratory for Chemical Biology of Fujian Province, Xiamen University, Xiamen, Fujian 361005, China.
State Key Laboratory of Physical Chemistry of Solid Surfaces and Fujian Provincial Key Laboratory of Theoretical and Computational Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, China.
Org Lett. 2021 Dec 17;23(24):9348-9352. doi: 10.1021/acs.orglett.1c03360. Epub 2021 Nov 30.
The visible-light-driven switchable phosphorylation of cyanoaromatics with the 1,6-enyne moiety for the diverse and selective synthesis of phosphorylated polyheterocycles, including phosphorylated aminophosphonates, iminophosphonates, and ketones, has been described. Importantly, these photocatalytic transformations feature good functional group tolerance and high regio- and chemoselectivities under mild reaction conditions. These findings might stimulate the exploration of new photocatalytic utilizations of P(O)-H compounds by employing CN-containing substrates as the radical acceptors.
可见光驱动的含 1,6-炔基部分的氰基芳烃的可切换磷酸化反应,用于各种和选择性的多杂环磷酸化化合物的合成,包括磷酸化的氨基膦酸酯、亚氨基膦酸酯和酮,已经被描述。重要的是,这些光催化转化在温和的反应条件下具有良好的官能团耐受性和高区域选择性和化学选择性。这些发现可能会刺激通过使用含 CN 的底物作为自由基受体来探索 P(O)-H 化合物的新的光催化利用。