Abstract:
When exposed to visible light, chloroform solutions of monothioanthraquinone and 2-methyl-10-monothioanthraquinone undergo photoconversion to form the oxidation products anthraquinones 2, α-hydroxyanthraquinones 3 and anthradioxathiapentalenes 4.
Document Type:
Article
Language: English
Citation:
V. A. Savel'ev, V. A. Loskutov, V. V. Shelkovnikov, “Photooxidation of Monothioanthraquinone and its 2-Methyl Derivative”, Mendeleev Commun., 3:2 (1993), 57–58
Linking options:
https://www.mathnet.ru/eng/mendc5265
https://www.mathnet.ru/eng/mendc/v3/i2/p57
This publication is cited in the following 2 articles:
Steven Mauries, Taylor O. Hope, Katie M. Psutka, Joshua Ledrew, Meghan Heer, Emma Guillet, Pedram Zand, Kenneth E. Maly, Mathieu Frenette, “Unusual Photochemistry in Aromatic Dithioimides: Quantitative Thione Reduction Promoted by Ether Solvents”, Chemistry A European J, 30:39 (2024)
V. A. SAVEL'EV, V. A. LOSKUTOV, V. V. SHELKOVNIKOV, “ChemInform Abstract: Photooxidation of Monothioanthraquinone and Its 2‐Methyl Derivative.”, ChemInform, 25:33 (1994)
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