Olivo Giorgio, Cussó Olaf, Costas Miquel
Departament de Química I Institut de Química Computacional i Catàlisi (IQCC), Universitat de Girona, Facultat de Ciències, Campus de Montilivi, Girona, 17071, Spain.
Chem Asian J. 2016 Nov 22;11(22):3148-3158. doi: 10.1002/asia.201601170. Epub 2016 Nov 15.
The development of catalysts for the selective oxidation of readily available hydrocarbons or organic precursors into oxygenated products is a long-standing goal in organic synthesis. In the last decade, some iron coordination complexes have shown the potential to fit this role. These catalysts can mimic the O-O activation mode of far more sophisticated iron oxygenase enzymes, generating powerful yet selective oxidants. In this review, we report state-of-the-art C-H and C=C oxidations catalyzed by non-heme iron complexes and H O as the oxidant. Finally, we briefly describe some novel oxidative reactivity and the perspectives of this chemistry.
开发能够将易于获得的碳氢化合物或有机前体选择性氧化为含氧化合物的催化剂,是有机合成领域长期以来的目标。在过去十年中,一些铁配位络合物已显示出胜任这一角色的潜力。这些催化剂可以模拟更为复杂的铁加氧酶的O - O活化模式,生成强效且具选择性的氧化剂。在本综述中,我们报道了以非血红素铁络合物和H₂O作为氧化剂催化的C - H和C = C氧化反应的最新进展。最后,我们简要描述了一些新颖的氧化反应活性以及该化学领域的前景。