Mao Bin, Fañanás-Mastral Martín, Feringa Ben L
Stratingh Institute for Chemistry, University of Groningen , Nijenborg 4, 9747 AG Groningen, The Netherlands.
National Engineering Research Center for Process Development of Active Pharmaceutical Ingredients, Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology , Hangzhou 310014, P. R. China.
Chem Rev. 2017 Aug 9;117(15):10502-10566. doi: 10.1021/acs.chemrev.7b00151. Epub 2017 Jun 22.
γ-Butenolides, γ-butyrolactones, and derivatives, especially in enantiomerically pure form, constitute the structural core of numerous natural products which display an impressive range of biological activities which are important for the development of novel physiological and therapeutic agents. Furthermore, optically active γ-butenolides and γ-butyrolactones serve also as a prominent class of chiral building blocks for the synthesis of diverse biological active compounds and complex molecules. Taking into account the varying biological activity profiles and wide-ranging structural diversity of the optically active γ-butenolide or γ-butyrolactone structure, the development of asymmetric synthetic strategies for assembling such challenging scaffolds has attracted major attention from synthetic chemists in the past decade. This review offers an overview of the different enantioselective synthesis of γ-butenolides and γ-butyrolactones which employ catalytic amounts of metal complexes or organocatalysts, with emphasis focused on the mechanistic issues that account for the observed stereocontrol of the representative reactions, as well as practical applications and synthetic potentials.
γ-丁烯内酯、γ-丁内酯及其衍生物,尤其是对映体纯形式的衍生物,构成了众多天然产物的结构核心,这些天然产物展现出一系列令人瞩目的生物活性,对新型生理和治疗药物的开发具有重要意义。此外,光学活性的γ-丁烯内酯和γ-丁内酯还是合成各种生物活性化合物和复杂分子的一类重要手性砌块。考虑到光学活性γ-丁烯内酯或γ-丁内酯结构的生物活性谱各不相同且结构多样性广泛,在过去十年中,用于构建此类具有挑战性骨架的不对称合成策略的开发引起了合成化学家的极大关注。本综述概述了使用催化量的金属配合物或有机催化剂对γ-丁烯内酯和γ-丁内酯进行的不同对映选择性合成,重点关注解释代表性反应中观察到的立体控制的机理问题,以及实际应用和合成潜力。