The Coupling of 4-Methoxy-2-naphthylamine with Diazotized Aminodiazo Thioethers*, 1

JS Hanker, L Katzoff, LD Aronson…

文献索引：Hanker,J.S. et al. Journal of Organic Chemistry, 1965 , vol. 30, p. 1779 - 1781

全文：HTML全文

被引用次数: 7

摘要

For the electron microscopic demonstration of aminopeptidase it would be desirable to incorporate an osmiophilic moiety6 such as the mercapto, thiocarbamyl, or diazo thioether group in the diazonium salt which couples with 4-methoxy-2-naphthylamine (11) produced by the action of the enzyme. Attempts to prepare diazonium compounds from mercaptoanilines with retention of the thiol group were unsuccessful. Attempts to prepare ...