Cui Xi-Yang, Tan Choon-Hong, Leow Dasheng
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore 637371.
Org Biomol Chem. 2019 May 15;17(19):4689-4699. doi: 10.1039/c8ob02240b.
Guanidines, which exist widely in nature, have been frequently utilised as strong Brønsted bases in organic chemistry. As ligands, guanidines can have different coordination modes with the metal center. However, the exploitation of these guanidine complexes as catalysts has been much less successful. The anionic counterpart of guanidine, which is known as guanidinate, is also able to function as a ligand. The catalytic activities of metal-guanidinate complexes are of great interest to chemists. The potential of catalytic guanidine or guanidinate metal complexes to catalyse unique chemical transformations is immensely promising. This field is currently being pursued with great interest by synthetic organic chemists. In this review, the representative reactions enabled by guanidine and guanidinate metal complexes are highlighted.
胍类化合物在自然界中广泛存在,在有机化学中常被用作强布朗斯特碱。作为配体,胍类化合物与金属中心可以有不同的配位模式。然而,将这些胍配合物用作催化剂的开发却不太成功。胍的阴离子对应物,即胍基负离子,也能够作为配体发挥作用。金属胍基负离子配合物的催化活性引起了化学家们的极大兴趣。催化胍或胍基金属配合物催化独特化学转化的潜力非常可观。目前,合成有机化学家对这一领域非常感兴趣。在这篇综述中,重点介绍了胍和胍基金属配合物实现的代表性反应。