SKELETAL REARRANGEMENT OF 2, 5-DIARYL-1, 4-DITHIIN-1-OXIDES INDUCED BY HYDROCHLORIC ACID
K Kobayashi, K Mutai
Index: Kobayashi, Keiji; Mutai, Kiyoshi Chemistry Letters, 1981 , p. 1105 - 1108
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Citation Number: 5
Abstract
Treatment of 2, 5-diphenyl-1, 4-dithiin-1-oxide with hydrochloric acid in dioxane caused a novel skeletal rearrangement to give 2-benzoyl-4-phenyl-1, 3-dithiole together with the deoxygenation products. The reaction with gaseous hydrogen chloride in methanol afforded the adduct due to the additive Pummerer rearrangement, which was also converted into the 1, 3-dithiole.
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