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- W3048990871 abstract "A regio‐ and chemoselective method for the preparation of 6‐trifluoromethyl‐5‐benzoyl‐2‐methylsulfanyl pyrimidines and their pyrimidin‐4(3 H )‐one analogues, from the cyclocondensation reaction of trifluoromethyl β‐enamino diketones with non‐symmetric 2‐methylisothiourea sulfates is reported. These diketones functioned as dual substrates by providing both products with high regioselectivity (only N 3 ‐substituted isomer was observed) and high chemoselectivity. A new feature provided by the starting material proposed herein is the possibility to either maintain or eliminate the trifluoromethyl group, by choosing the solvent." @default.
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- W3048990871 date "2020-08-14" @default.
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- W3048990871 title "Trifluoromethyl β‐Enamino Diketones as Dual Substrates for the Synthesis of 5‐Benzoyl‐6‐(trifluoromethyl)pyrimidines and their Pyrimidin‐4(3 <i>H</i> )‐one Analogues" @default.
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- W3048990871 doi "https://doi.org/10.1002/ejoc.202000879" @default.
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