Abstract:Die Umsetzung der Aminodiphenyläther (I) mit aromatischen Aldehyden wie z.B. (II) in Benzol führt zu den Azomethinen (III), die ohne Isolierung mit überschüssiger Thioglykolsäure (IV) zu den Titelverbindungen (V) cyclisiert werden.
“…Solvents and common reagents obtained from Merck and Aldrich, were of reagent grade. Thiazolidinones 2e-g and benzylidene derivative 3g were prepared by literature procedures [8,9] and the spectral data are in agreement with that given in the literature.…”
Alkyl and aryl substituted furothiazolidine derivatives have been synthesized by the reaction of Wittig reagent with benzylidene derivatives of 4‐thiazolidinones obtained from aldimines and thioglicolic acid.
“…Solvents and common reagents obtained from Merck and Aldrich, were of reagent grade. Thiazolidinones 2e-g and benzylidene derivative 3g were prepared by literature procedures [8,9] and the spectral data are in agreement with that given in the literature.…”
Alkyl and aryl substituted furothiazolidine derivatives have been synthesized by the reaction of Wittig reagent with benzylidene derivatives of 4‐thiazolidinones obtained from aldimines and thioglicolic acid.
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