Acetals of lactams and acid amides. 67. Polarographic behavior of enamines of the indoles series in anhydrous DMF

Autor:	O. A. Petrishcheva, V. G. Granik, M. K. Polievktov, T. V. Golovko, S. Yu. Ryabova
Rok vydání:	1991
Předmět:	Indole test Polarography chemistry.chemical_compound chemistry Organic Chemistry Anhydrous Substituent chemistry.chemical_element Organic chemistry Nitrogen Enamine
Zdroj:	Chemistry of Heterocyclic Compounds. 27:511-516
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00473996
Popis:	The polarographic behavior of derivatives of 2-aminomethyleneindoxyl and 3-aminomethyleneoxindole in anhydrous DMF has been studied and the results compared with data on the polarographic reduction of substituted aminomethyleneacetophenones and of related enaminoketones and eneaminoamides. It is established that the ease of reduction is determined by the nature of the substituent on the enamine and indole nitrogen atoms and also by the presence or absence of an α-methyl group in the α-position of the eneamines (for noncyclic enaminoketones).
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ee5cf40a0cf463b9b1b5f23d1363bfae https://doi.org/10.1007/bf00473996 Zobrazit plný text záznamu Full text from SpringerLink