The oxidation of ethane-1,2-diol resulting from molecular oxygen activation by copper: formation of an oxoethanoate complex precedes carbon–carbon bond cleavage
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930001698
Reference8 articles.
1. Reactivity of metallic copper with acidic organic compounds in the presence of molecular oxygen. Crystal structure of [{Cu(NCO)(py)2}2]·H2O
2. N. Ravasio , M.Gargano and M.Rossi, New Developments in Selective Oxidation, ed. G. Centi and F. Trifirò, Elsevier, Amsterdam, 1990, p. 139.
3. K. D. Karlin and J.Zubieta, Copper Coordination Chemistry: Biochemical and Inorganic Perspective, Adenine Press, Guilder-land, NY, 1983.
4. Copper(II)-induced oxidations of aromatic substrates: catalytic conversion of catechols to o-benzoquinones. Copper phenoxides as intermediates in the oxidation of phenol, and a single-step conversion of phenol, ammonia, and oxygen into muconic acid mononitrile
5. A square-pyramidal copper complex containing both monodentate and anti-syn bridging formate groups: crystal structure of catena-μ-formato-formatobis(pyridine)copper(II) monohydrate
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