Wu Yingtao, Pi Chao, Cui Xiuling, Wu Yangjie
Green Catalysis Center and College of Chemistry , Zhengzhou University , No. 75 Daxue Road , Zhengzhou , Henan 450052 , P. R. China.
Org Lett. 2020 Jan 17;22(2):361-364. doi: 10.1021/acs.orglett.9b03768. Epub 2020 Jan 2.
A novel synthesis of 3-nitrosoindoles starting from easily available -nitrosoanilines and sulfoxonium ylides via Rh(III)-catalyzed acylmethylation and trifluoroacetic acid (TFA)-mediated nitroso transfer/cyclization cascade reaction in one pot has been developed. The -nitroso group plays a dual role as a versatile directing group and internal nitrosation reagent. Rh(III)-catalyzed C-H activation/C-C bond formation and TFA-mediated N-N bond cleavage/formation of two C-N bonds are involved in this reaction. This process is scalable and avoids external oxidation. DMSO and HO are produced as byproducts. Moreover, further chemical transformations of the desired products enhance its synthetic value.
已开发出一种从易于获得的亚硝基苯胺和亚砜叶立德出发,通过铑(III)催化的酰甲基化和三氟乙酸(TFA)介导的亚硝基转移/环化串联反应一锅法合成3-亚硝基吲哚的新方法。亚硝基作为通用导向基团和内部亚硝化试剂发挥双重作用。该反应涉及铑(III)催化的C-H活化/C-C键形成以及TFA介导的N-N键断裂/两个C-N键的形成。此过程可扩展且避免了外部氧化。副产物为二甲基亚砜和水。此外,所需产物的进一步化学转化提高了其合成价值。