Syntheses of 9,10-Phenanthrenequinone and 9-Methoxyphenanthrene by Oxidation of Phenanthrene with Dihydroxy Phenylselenonium Benzenesulfonate
- 1 January 1997
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 27 (1) , 89-94
- https://doi.org/10.1080/00397919708004809
Abstract
9,10-Phenanthrenequinone is prepared by oxidation of phenanthrene with dihydroxy phenylselenonium benzenesulfonate in boiling dioxane-water. 9-methoxyphenanthrene is obtained when the reaction is carried out in methanol.Keywords
This publication has 10 references indexed in Scilit:
- Dihydroxy Phenylselenoniump-Toluenesulfonate; Preparation and Use in the Recycling of Selenium ReagentsSynthetic Communications, 1996
- Competing ene-reactions in the p-oxidation and o-phenylselenylation of phenol with benzeneseleninic acidTetrahedron Letters, 1994
- Quinolinium Fluorochromate (QFC), C9H7NH[CrO3F]: An Improved Cr(VI)-Oxidant for Organic SubstratesBulletin of the Chemical Society of Japan, 1994
- Electrophilic phenylselenenylation of thiophenes. Synthesis of poly(phenylseleno)thiophenes.Tetrahedron, 1994
- Oxidative Cleavage of Diselenide by m-Nitrobenzenesulfonyl Peroxide. Novel Method for the Electrophilic Benzeneselenenylations of Olefins and Aromatic RingsBulletin of the Chemical Society of Japan, 1991
- Selenium-catalyzed conversion of methyl ketones into .alpha.-keto acetalsThe Journal of Organic Chemistry, 1990
- Reactions of Alkenediazonium Salts. Part 2. Methanolysis of 2,2(2′,2″‐biphenylylene)ethene‐1‐diazonium hexachloroantimonate. A rearrangement to 9‐methoxyphenanthreneHelvetica Chimica Acta, 1983
- Direct selenation of electron-rich aromatic compounds with (phenylseleno)dimethylsulfonium tetrafluoroborateThe Journal of Organic Chemistry, 1982
- The Action of Phenylmagnesium Bromide on 10,10-Diphenyl-9,10-dihydro-9-phenanthrone1Journal of the American Chemical Society, 1957
- The Reaction of Fluorenone and Diazomethane—A New Route to 9-Phenanthrol DerivativesJournal of the American Chemical Society, 1940