ON THE SYNTHESIS OF MONOMERIC METHACRYLOYLAMINO DERIVATIVES OF PURINE BASES

Abstract
Three sorts of methacryloylamino derivatives of adenine and theophylline were prepared by allowing 9-(2-aminoethyl)adenine and 7-(2-aminoethyl)theophylline to react with methacryloyl chloride in dimethylformamide-pyridine solution at room temperature. Free-radical polymerization and copolymerization of 7-(2-methacryloylaminoethyl)theophylline were studied.

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