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Abstract Formylation of 6-methyl-2 S -substituted pyrimidin-4-ols under the conditions of the Vilsmeier–Haack reaction leads to the formation of nucleophilic substitution products of the hydroxyl group. The formation of the… Click to show full abstract
Abstract Formylation of 6-methyl-2 S -substituted pyrimidin-4-ols under the conditions of the Vilsmeier–Haack reaction leads to the formation of nucleophilic substitution products of the hydroxyl group. The formation of the expected formylation products does not occur.
Keywords:
methyl substituted;
substituted pyrimidin;
pyrimidin ols;
vilsmeier haack
Journal Title: Russian Journal of General Chemistry
Year Published: 2020
Link to full text (if available)
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Journal Title: Russian Journal of General Chemistry
Year Published: 2020
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!