Department of Chemistry, Rutgers University, 73 Warren Street, Newark, New Jersey 07102, United States.
Org Lett. 2021 Jun 18;23(12):4818-4822. doi: 10.1021/acs.orglett.1c01535. Epub 2021 Jun 7.
The direct synthesis of sulfoxonium ylides from amides by selective N-C(O) cleavage is presented. The reaction proceeds through the nucleophilic addition of dimethylsulfoxonium methylide to the amide bond in acyclic twisted amides under exceedingly mild room temperature conditions. A variety of amides can be employed, and the protocol can be applied to the late-stage derivatization of pharmaceuticals. Mechanistic studies outline the relative order of reactivity of amides.
本文报道了一种通过选择性 N-C(O)裂解从酰胺直接合成亚磺酰基叶立德的方法。该反应在极其温和的室温条件下,通过二甲亚砜甲基叶立德对非环扭曲酰胺中的酰胺键进行亲核加成来进行。各种酰胺都可以被使用,该方法可以应用于药物的后期衍生化。机理研究概述了酰胺的相对反应活性顺序。