Abstract
In the presence of stannic chloride, 2,3-dichlorotetrahydrofuran adds to isoprene with the formation of 3-chloro-2-(4′-chloro-2′-methylbut-2′-enyl)tetrahydrofuran and to piperylene and bivinyl with the formation, predominantly, of 3-chloro-2-(4′-chloropent-2′-enyl)- and 3-chloro-2′-(4′-chlorobut-2′-enyl)tetrahydrofuran, respectively, with their allyl isomers. The amount of the latter was estimated from the NMR spectra at 20–30%.
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For part VII, see [1].
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Tarnopol'skii, Y.I., Nadelyaeva, A.K. Investigations in the field of oxygen-containing heterocycles. Chem Heterocycl Compd 5, 1–3 (1969). https://doi.org/10.1007/BF01031746
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DOI: https://doi.org/10.1007/BF01031746