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- W2949657908 abstract "Reaction of 4-chloro-3′-methylthio-3,4′-diquinolinyl sulfides 3, 9b, 9c with a nitrating mixture proceeds via the 3′-methylthio group monooxidation and yields 3′-methylsulfinyl diquinolinyl sulfides 4, 5b, 5c, respectively. Further treatment of 4 with a nitrating mixture followed as C5- and C8-nitration and gives mixture of 5a and 5c. Treatment of 3′-methylsulfinyl quinolines 6 and 7 with hydrochloric acid/potassium iodide system causes reduction of the sulfoxide group in 6 and 7 to the sulfide group yielding 8, in case of 4-methoxyquinolines 6, hydrolysis of the 4-methoxyquinoline moiety to the 4-quinolinone moiety takes place simultaneously. The proton and carbon chemical shifts of 4 and 5a were completely assigned following COSY, HETCOR and INEPT or COLOC studies." @default.
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- W2949657908 date "2000-07-01" @default.
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- W2949657908 title "4-Chloro-3′-methylsulfinyl-5(6 or 8)-nitro-3,4′-diquinolinyl sulfides" @default.
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- W2949657908 doi "https://doi.org/10.1002/jhet.5570370404" @default.
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