Xu Hongtao, Ma Fei, Wang Nan, Hou Wei, Xiong Huan, Lu Fengping, Li Jie, Wang Shuyue, Ma Peixiang, Yang Guang, Lerner Richard A
Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
College of Pharmaceutical Science and Institute of Drug Development & Chemical Biology (IDD & CB) Zhejiang University of Technology Hangzhou 310014 China.
Adv Sci (Weinh). 2019 Sep 30;6(23):1901551. doi: 10.1002/advs.201901551. eCollection 2019 Dec.
Using (hetero)aryl fluorosulfonates as versatile electrophiles, facile on-DNA cross-coupling reactions of Suzuki, Sonogashira, and Buchwald are reported here. Notably, all of these reactions show excellent functional group tolerance, mild reaction conditions (relative low temperature and open to air), rich heterocyclic coupling partners, and more importantly, DNA-compatibility. Thus, these new reactions based on efficient formation of C(sp)-C(sp), C(sp)-C(sp), and C(sp)-N bonds are highly amenable to synthesis of DNA-encoded libraries with great molecular diversity.
本文报道了使用(杂)芳基氟磺酸盐作为通用亲电试剂,实现了铃木(Suzuki)、索尼加什拉(Sonogashira)和布赫瓦尔德(Buchwald)反应在DNA上的简便交叉偶联反应。值得注意的是,所有这些反应都表现出优异的官能团耐受性、温和的反应条件(相对低温且可在空气中进行)、丰富的杂环偶联伙伴,更重要的是,具有DNA兼容性。因此,这些基于高效形成C(sp)-C(sp)、C(sp)-C(sp)和C(sp)-N键的新反应非常适合合成具有高度分子多样性的DNA编码文库。