A One-Pot Synthesis of 1-(2,2,6,6-tetramethyl-4-piperidinyl)-4-(4-fluorophenyl)-5-(2-amino-4- pyrimidinyl)-imidazole: A Potent Inhibitor of P38 MAP Kinase
Synthesis for 4-aryl-5-pyrimidine imidazole substituted derivatives
The present invention relates to a novel method for synthesizing imidazole derivatives having 4-aryl, 5-pyrimidine heterocyclic rings using a novel cycloaddition reaction.
The present invention relates to a novel method for synthesizing imidazole derivatives having 4-aryl, 5-pyrimidine heterocyclic rings using a novel cycloaddition reaction.
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(2008/06/13)
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