An efficient synthesis of thiazolo[3,2-a]pyrimidinones
Review articleOpen access

AbstractA series of thiazolo[3,2-a]pyrimidinones was synthesised in a two-step procedure, using Eaton’s reagent to effect cyclisation of 2-aminothiazoles. The use of relatively low temperatures, facile product isolation and short reaction times make this cyclisation procedure a particularly attractive option over more conventional methods.

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