Metal-catalysed reactions enabled by guanidine-type ligands

被引:50
|
作者
Cui, Xi-Yang [1 ]
Tan, Choon-Hong [1 ]
Leow, Dasheng [1 ]
机构
[1] Nanyang Technol Univ, Div Chem & Biol Chem, Sch Phys & Math Sci, 21 Nanyang Link, Singapore 637371, Singapore
关键词
RING-OPENING POLYMERIZATION; TRANSFER RADICAL POLYMERIZATION; COPPER-COMPLEXES; ASYMMETRIC ALKYNYLATION; BIOLOGICAL OXIDATION; CRYSTAL-STRUCTURE; ROOM-TEMPERATURE; PHASE-TRANSFER; H INSERTION; CHEMISTRY;
D O I
10.1039/c8ob02240b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Guanidines, which exist widely in nature, have been frequently utilised as strong Bronsted 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.
引用
收藏
页码:4689 / 4699
页数:11
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