Abstract
1-Allyloxy-2-allylthio-4-methylbenzene rearranges in NN-diethylaniline at 215°C with migration of allyloxy and allylthio groups to form 2,4-dimethyl-6-allyl-7-hydroxy-2,3dihydrobenzothiophene.
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Additional information
M. V. Lomonosov State University, Moscow 119899. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 480–482, 1994. Original article submitted March 5, 1994.
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Anisimov, A.V., Grishkyan, A.A., Gaisina, K.A. et al. Rearragnement of 1-allyloxy-2-allylthio-4-methyl-benzene TO 2,4-dimethyl-6-allyl-7 hydroxy-2,3-dihydrobenzothiophene. Chem Heterocycl Compd 30, 420–421 (1994). https://doi.org/10.1007/BF01169934
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DOI: https://doi.org/10.1007/BF01169934