Evgeny M. Buev, Anna P. Osintseva, V. Moshkin
Sep 1, 2020
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Journal
Chemistry of Heterocyclic Compounds
Abstract
The reaction of aryl isothiocyanates with nonstabilized azomethine ylides generated in situ by various methods was studied. It was established that the use of N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine in the presence of trifluoroacetic acid in the role of a catalyst led to the formation of (Z)-N-aryl-3-benzylthiazolidin-5-imines in 22–47% yields.