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- W2041252178 endingPage "1932" @default.
- W2041252178 startingPage "1921" @default.
- W2041252178 abstract "In the presence of acid the dimer 1 of 3-hydroxy-2,3-dimethylindolenine rearranges to 4, and then via 6 to 7a which is cleaved to 2,3-dimethylindole (2) and 2-formyl-3-methylindole (3). If peroxides and oxygen are not excluded, two other products, 13 and 30, are also formed. A rationalization of these reactions is offered which takes into account subtle differences in migratory aptitudes." @default.
- W2041252178 created "2016-06-24" @default.
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- W2041252178 date "1971-06-01" @default.
- W2041252178 modified "2023-09-24" @default.
- W2041252178 title "Complex Rearrangements of the Dimer of 3-Hydroxy-2,3-dimethylindolenine" @default.
- W2041252178 doi "https://doi.org/10.1139/v71-311" @default.
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