The chemotherapy of schistosomiasis. Part VIII. 2-Carboxy- and 2-carbamoyl-4-aminophenyl ethers
作者:R. F. Collins、M. Davis
DOI:10.1039/j39660002196
日期:——
Synthetic work in the series of schistosomicidal p-aminophenyl ethers has been continued with the introduction of carboxy-, carbamoyl-, alkylsulphonyl-, and some miscellaneous nuclear substituents for structure–activity studies.
The chemotherapy of schistosomiasis. Part VII. 2-Methyl- and 2-(substituted methyl)-4-aminophenyl ethers
作者:R. F. Collins、M. Davis
DOI:10.1039/j39660000873
日期:——
Chloromethylation of p-nitrophenol or its alkyl ethers gave reactive 2-chloromethyl intermediates which have been converted into 2-hydroxymethyl-(VII), 2-mercaptomethyl-(II), or 2-aminomethyl-4-nitrophenyl ethers (X), and various acyl, alkyl, aryl, and sulphone derivatives. The amines (VIII) obtained on reduction have been studied as schistosomicides.