Arii Suguru, Yu Zonghan, Chen Hongyu, Mitsunuma Harunobu, Kanai Motomu
Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Angew Chem Int Ed Engl. 2025 May;64(21):e202503249. doi: 10.1002/anie.202503249. Epub 2025 Mar 16.
We report a catalytic allylation of ketones using simple hydrocarbon alkenes, enabled by a synergistic system comprising chromocene and photo-activatable ion-pair hydrogen atom transfer (IP-HAT) catalysts derived from a thiophosphoryl imide and N-heteroaromatics. This catalyst system generates highly nucleophilic, electron-rich allylchromium(III) species directly from unactivated alkenes, demonstrating broad applicability to various ketones, including aromatic, aliphatic, and multifunctional ketones. The reaction proceeds under mild conditions with high functional group tolerance. The modular design of the IP-HAT catalysts allows precise tuning of redox potential and HAT activity, with the enhanced reduction potential of the reduced N-heteroaromatics catalyst playing a pivotal role in efficiently regenerating the electron-rich chromocene(II) catalyst.
我们报道了一种使用简单烃类烯烃对酮进行催化烯丙基化反应的方法,该反应由一种协同体系实现,该体系包含二茂铬以及由硫代磷酰亚胺和氮杂芳烃衍生的光可活化离子对氢原子转移(IP-HAT)催化剂。这种催化剂体系能直接从未活化的烯烃生成高亲核性、富电子的烯丙基铬(III)物种,证明了其对各种酮具有广泛适用性,包括芳香族、脂肪族和多功能酮。该反应在温和条件下进行,对官能团具有高耐受性。IP-HAT催化剂的模块化设计允许对氧化还原电位和HAT活性进行精确调节,还原态氮杂芳烃催化剂增强的还原电位在有效再生富电子二茂铬(II)催化剂中起着关键作用。