REACTION OF <i>N</i>-BENZYL AZOMETHINE YLIDE WITH ARYL ISOTHIOCYANATES: SYNTHESIS OF (<i>Z</i>)-<i>N</i>-ARYL-3-BENZYLTHIAZOLIDINE-5-IMINES
DOI:
https://doi.org/10.1007/5621Keywords:
azomethine ylides, isothiocyanates, thiazolidines, [3 2] cycloadditionAbstract
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.
Authors: Evgeny M. Buev*, Anna P. Osintseva, Vladimir S. Moshkin, Vyacheslav Ya. Sosnovskikh
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Published
2020-10-14
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Short Communications