Yang Shu, Guo Ting-Ting, Ma Jian-Bo, Jia Hui-Ting, Liu Jin, Yan Sheng-Jiao
Key Laboratory of Medicinal Chemistry for Natural Resource (Yunnan University), Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, P. R. China.
J Org Chem. 2024 Sep 20;89(18):13678-13690. doi: 10.1021/acs.joc.4c01899. Epub 2024 Sep 6.
Herein, a visible-light-promoted radical cascade cyclization of heterocyclic ketene aminals (HKAs) and thiocyanates was developed to access functionalized fused 2-iminothiazolines. This novel cascade reaction can be realized under only visible-light irradiation without the help of external photocatalysts, oxidants, and additives. These multicomponent cascade reactions demonstrate excellent selectivity for the -isomers and ensure the formation of the products only in their isomeric form. Preliminary mechanism investigations demonstrated that HKAs and thiocyanates can form electron donor-acceptor complexes for harvesting the energy of visible light to activate substrates and generate reactive radicals. This protocol can be used for synthesizing various natural-like products such as fused 2-iminothiazolines. This approach demonstrates multiple advantages such as commercially available substrates, convenient operation, environmentally friendly, mild conditions, and an efficient multicomponent reaction (2A + B).
在此,我们开发了一种可见光促进的杂环烯酮缩胺(HKAs)与硫氰酸盐的自由基级联环化反应,用于合成功能化稠合2-亚氨基噻唑啉。这种新型级联反应仅在可见光照射下即可实现,无需外部光催化剂、氧化剂和添加剂的帮助。这些多组分级联反应对β-异构体表现出优异的选择性,并确保仅以其异构体形式形成产物。初步机理研究表明,HKAs和硫氰酸盐可以形成电子供体-受体复合物,以收集可见光的能量来活化底物并产生活性自由基。该方法可用于合成各种类天然产物,如稠合2-亚氨基噻唑啉。这种方法具有多种优点,如底物可商购、操作简便、环境友好、条件温和以及高效的多组分反应(2A + B)。