フェナントリヂン誘導体の研究 (第6報)
1952 年 72 巻 3 号 p. 344-346
詳細
1952 年 72 巻 3 号 p. 344-346
It was concluded from the experiments conducted that the by-product obtained in the Pschorr cyclization of 2-aminopiperonoyl-N-benzylaniline and 2-aminobenzoyl-N-benzyl-p-phenetidine is the dimer formed by condensation, with liberation of nitrogen, at the amino group of the original material which undergoes diazotization.
