Pu Yiru, Wang Maolin, Tian Wanrong, Ge Xian, Zhu Dikai, Wang Chuanqi, Zeng Yingjie, Tao Feiyan, Deng Yun, Lu Jun
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine Chengdu 611137 China
Clinical Research Center, The First Affiliated Hospital of Shantou University Medical College Shantou Guangdong Province 515000 China.
RSC Adv. 2024 Jun 10;14(26):18453-18458. doi: 10.1039/d4ra02252a. eCollection 2024 Jun 6.
Asymmetric catalytic processes promoted by N-heterocyclic carbenes (NHCs) hold great potential for the sustainable preparation of chiral molecules. However, catalyzing the reactions by manipulating the reactive intermediates is challenging. We report herein that the known NHC-catalyzed [3 + 2] annulation reaction between ketimine and enal can also be turned into a [2 + 3] annulation reaction for the highly enantioselective direct synthesis of trifluoroethyl 3,2'-spirooxindole γ-lactams (4) through timely catalysis of the intermediates. DFT calculations revealed that this transformation included the key step of the nucleophilic attack of the Breslow intermediate M2 derived from NHC and enal (2) to the unattacked ketimine (1). Our study demonstrates that it is possible to tune the desired selectivities through the dynamic catalysts of the reactive intermediates.
由氮杂环卡宾(NHCs)促进的不对称催化过程在手性分子的可持续制备方面具有巨大潜力。然而,通过操纵反应中间体来催化反应具有挑战性。我们在此报告,已知的NHC催化的酮亚胺与烯醛之间的[3 + 2]环化反应也可以通过对中间体的适时催化转化为[2 + 3]环化反应,用于高对映选择性直接合成三氟乙基3,2'-螺环氧化吲哚γ-内酰胺(4)。密度泛函理论计算表明,这种转化包括源自NHC和烯醛(2)的布雷斯洛中间体M2对未反应的酮亚胺(1)进行亲核进攻的关键步骤。我们的研究表明,通过反应中间体的动态催化剂来调节所需的选择性是可能的。