Stevens rearrangement of heterocyclic ammonium salts containing prop-2-yn-1-yl group

Autor:	G. T. Sargsyan, J. V. Grigoryan, A. M. Petrosyan, A. Kh. Gyul’nazaryan, G. A. Panosyan, T. A. Sahakyan, G. M. Muradyan
Rok vydání:	2016
Předmět:	010405 organic chemistry General Chemistry Hydrogen atom 010402 general chemistry Phenacyl 01 natural sciences Medicinal chemistry 0104 chemical sciences chemistry.chemical_compound Stevens rearrangement chemistry Group (periodic table) Furan Organic chemistry Moiety Ammonium
Zdroj:	Russian Journal of General Chemistry. 86:2067-2070
ISSN:	1608-3350 1070-3632
DOI:	10.1134/s1070363216090140
Popis:	Stevens rearrangement was studied of ammonium salts where piperidinium or morpholinium groups are linked to prop-2-yn-1-yl moiety and labile hydrogen atom functions (methoxycarbonylmethyl, phenacyl, cyanomethyl). In the case of phenacyl analog furan derivatives were formed, in other cases dienamines were the reaction products.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::4127fc8756f79d069baf025ac4891f86 https://doi.org/10.1134/s1070363216090140 Zobrazit plný text záznamu Plný text ve formátu PDF