Synthesis of novel pyridine and pyrimidine derivatives as potential inhibitors of HIV-1 reverse transcriptase using palladium-catalysed C-N cross-coupling and nucleophilic aromatic substitution reactions
Synthesis of novel pyridine and pyrimidine derivatives as potential inhibitors of HIV-1 reverse transcriptase using palladium-catalysed C-N cross-coupling and nucleophilic aromatic substitution reactions
2,4,6-trichloropyrimidine. Reaction with 4-substituted phenolate ions
作者:Thomas J. Delia、A. Nagarajan
DOI:10.1002/jhet.5570350201
日期:1998.3
A systematic investigation of the reactivity of 2,4,6-trichloropyrimidine with phenoxide nucleophiles has been conducted. Conditions have been described which lead to mono-, di-, and trisubstituted-pyrimidines. Unexpected product distributions for mono- and disubstituted products were observed and explanations for these results are offered.