Department of Chemistry, Stanford University, Stanford, CA 94305-5080 (USA).
Angew Chem Int Ed Engl. 2015 Apr 20;54(17):5026-43. doi: 10.1002/anie.201411073. Epub 2015 Mar 20.
Nitrogen-, phosphorus-, and oxygen-based ligands with chiral backbones have been the historic workhorses of asymmetric transition-metal-catalyzed reactions. On the contrary, sulfoxides containing chirality at the sulfur atom have mainly been used as chiral auxiliaries for diastereoselective reactions. Despite several distinct advantages over traditional ligand scaffolds, such as the proximity of the chiral information to the metal center and the ability to switch between S and O coordination, these compounds have only recently emerged as a versatile class of chiral ligands. In this Review, we detail the history of the development of chiral sulfoxide ligands for asymmetric catalysis. We also provide brief descriptions of metal-sulfoxide bonding and strategies for the synthesis of enantiopure sulfoxides. Finally, insights into the future development of this underutilized ligand class are discussed.
氮、磷和氧为基础的配体具有手性骨架,一直是不对称过渡金属催化反应的历史主力。相反,含手性硫原子的亚砜主要用作非对映选择性反应的手性助剂。尽管与传统配体骨架相比具有几个明显的优势,例如手性信息与金属中心的接近性以及在 S 和 O 配位之间切换的能力,但这些化合物直到最近才作为一类多功能的手性配体出现。在这篇综述中,我们详细介绍了手性亚砜配体在不对称催化中的发展历史。我们还简要描述了金属-亚砜键合以及手性纯亚砜合成的策略。最后,讨论了这个未充分利用的配体类别的未来发展前景。