Abstract
On reaction with N-phenylethyleneimine in the presence of tetraethylammonium bromide, methyl and phenyl isothiocyanates form 2-methyl- and 2-phenyl-imino-3-phenylthiazolidines. In this reaction, methyl isothiocyanate partially trimerizes. Under the action of N-phenylethyleneimine phenylisocyanate trimerizes in high yield.
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For part I, see [9].
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Sineokov, A.P., Gladysheva, V.N. & Etlis, V.S. Cleavage of the aziridine ring. Chem Heterocycl Compd 4, 418–420 (1968). https://doi.org/10.1007/BF00755307
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DOI: https://doi.org/10.1007/BF00755307