Oxydation selective en para des phenols par un complexe cuivrique oxydant
P Capdevielle, M Maumy
Index: Capdevielle, Patrice; Maumy, Michel Tetrahedron Letters, 1983 , vol. 24, # 50 p. 5611 - 5614
Full Text: HTML
Citation Number: 36
Abstract
Abstract Oxidation of phenols by molecular oxygen in the presence of the μ-oxo cupric catalyst Cu 4 Cl 4 O 2 (CH 3-CN) 3 (A), can be selectively directed to give either oxidative coupling or para-hydroxylation (p-quinols or p-quinones) products by the choice of the (A)/(phenol) ratio. The mechanism is discussed and a-OH ligand transfer from Cu II to the phenolic para position is proposed.
Related Articles:
[Iwasa, Seiji; Fakhruddin, Ahmad; Widagdo, Herman Setyo; Nishiyama, Hisao Advanced Synthesis and Catalysis, 2005 , vol. 347, # 4 p. 517 - 520]
Allylation and oxidation reactions promoted by cobalt (II) complexes
[Gaudemer, A.; Nguyen-Van-Duong, K.; Shahkarami, N.; Achi, S. S.; Frostin-Rio, M.; Pujol, D. Tetrahedron, 1985 , vol. 41, # 19 p. 4095 - 4106]
On the regioselectivity of the fremy's salt oxidation of phenols
[Deya, Pedro M.; Dopico, Mercedes; Raso, Angel Garcia; Morey, Jeronimo; Saa, Jose M. Tetrahedron, 1987 , vol. 43, # 15 p. 3523 - 3532]
[Zagulyaeva, Aleksandra A.; Banek, Christopher T.; Yusubov, Mekhman S.; Zhdankin, Viktor V. Organic Letters, 2010 , vol. 12, # 20 p. 4644 - 4647]
[Ali, Mohammed Hashmat; Niedbalski, Melinda; Bohnert, Gary; Bryant, Daniel Synthetic Communications, 2006 , vol. 36, # 12 p. 1751 - 1759]