Literature DB >> 31032829

Metal-catalysed reactions enabled by guanidine-type ligands.

Xi-Yang Cui1, Choon-Hong Tan, Dasheng Leow.   

Abstract

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.

Entities:  

Year:  2019        PMID: 31032829     DOI: 10.1039/c8ob02240b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Enantioselective [1,2]-Stevens rearrangement of thiosulfonates to construct dithio-substituted quaternary carbon centers.

Authors:  Linfeng Hu; Jinzhao Li; Yongyan Zhang; Xiaoming Feng; Xiaohua Liu
Journal:  Chem Sci       Date:  2022-03-11       Impact factor: 9.825

2.  Enantioselective carbene insertion into the N-H bond of benzophenone imine.

Authors:  Jian Yang; Peiran Ruan; Wei Yang; Xiaoming Feng; Xiaohua Liu
Journal:  Chem Sci       Date:  2019-09-18       Impact factor: 9.825

  2 in total

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