Chemical Technology Division, CSIR-IHBT, Palampur, HP 176 061, India.
Org Biomol Chem. 2021 May 12;19(18):4014-4026. doi: 10.1039/d1ob00232e.
In the last two decades tremendous progress has been made in transition-metal (TM)-catalyzed C-H bond functionalization, paving the way to design complex molecules. Despite significant advances, enantioselective C-H activation is still in the age of infancy. For the enantioselective synthesis, several TM catalyst based approaches are well known, including kinetic resolution (KR) and its advanced versions [dynamic kinetic resolution (DKR) and parallel kinetic resolution (PKR)]. These strategies have recently been successfully applied synergetically with the TM catalyzed C-H activation to achieve enantioselective synthesis in a more economical and sustainable way. This review will summarize the recent advancements made towards merging KR with TM-catalysed C-H activation for enantioselective synthesis.
在过去的二十年中,过渡金属(TM)催化的 C-H 键功能化取得了巨大的进展,为设计复杂分子铺平了道路。尽管取得了重大进展,但对映选择性 C-H 活化仍然处于起步阶段。对于对映选择性合成,有几种基于 TM 催化剂的方法是众所周知的,包括动力学拆分(KR)及其高级版本[动态动力学拆分(DKR)和并行动力学拆分(PKR)]。这些策略最近已成功协同 TM 催化的 C-H 活化应用于以更经济和可持续的方式实现对映选择性合成。本文综述了将 KR 与 TM 催化的 C-H 活化相结合用于对映选择性合成的最新进展。