Jiangsu Key Laboratory of Pesticide Science, College of Sciences, Nanjing Agricultural University, Nanjing 210095, China.
State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071, China.
Org Lett. 2020 Dec 18;22(24):9638-9643. doi: 10.1021/acs.orglett.0c03703. Epub 2020 Dec 7.
An electron donor-acceptor complex-initiated α-cyanation of tertiary amines has been described. The reaction protocol provides a novel method to synthesize various α-amino nitriles under mild conditions. The reaction can proceed smoothly without the presence of photocatalysts and transition metal catalysts, and either oxidants are unnecessary or O is the only oxidant. The practicality of this method is showcased not only by the late-stage functionalization of natural alkaloid derivatives and pharmaceutical intermediate, but also by the applicability of a stop-flow microtubing reactor.
本文描述了一种由电子给体-受体复合物引发的叔胺的α-氰化反应。该反应方案提供了一种在温和条件下合成各种α-氨基腈的新方法。该反应可以在没有光催化剂和过渡金属催化剂的情况下顺利进行,并且不需要氧化剂或只有 O 是氧化剂。这种方法的实用性不仅体现在天然生物碱衍生物和药物中间体的后期官能化方面,还体现在停流微管反应器的适用性方面。