Faculty of Education, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 903-0213, Japan.
Molecules. 2019 Feb 25;24(4):824. doi: 10.3390/molecules24040824.
Phthalides and α,β-butenolides are two related classes of oxygenated heterocycles with a wide range of biological activities. An innovative strategy to prepare these compounds is based on C-H bond functionalization reactions, in which two simple, unfunctionalized molecules are coupled together with cleavage of a C-H bond and formation of a C-X bond (X=C or heteroatom). This paper reviews the methods for the synthesis of phthalides and α,β-butenolides by C-H bond functionalization from non-halogenated starting materials. Over 30 methods are reported, mostly developed during the past ten years.
苯酞和α,β-丁烯内酯是两类具有广泛生物活性的含氧杂环化合物。一种制备这些化合物的创新策略是基于 C-H 键功能化反应,其中两个简单的、未官能化的分子通过 C-H 键的断裂和 C-X 键(X=C 或杂原子)的形成而偶联在一起。本文综述了通过非卤代原料的 C-H 键功能化来合成苯酞和α,β-丁烯内酯的方法。报道了 30 多种方法,其中大多数是在过去十年中开发的。