Reaction of alkene oxides with aromatic thionylimines

Autor:	V. S. Etlis, A. P. Sineokov, M. E. Sergeeva
Rok vydání:	1968
Předmět:	chemistry.chemical_classification Ethylene Alkene Organic Chemistry Chloride Propene chemistry.chemical_compound Thionyl chloride chemistry Bromide Polymer chemistry medicine Organic chemistry Epichlorohydrin Tetraethylammonium bromide medicine.drug
Zdroj:	Chemistry of Heterocyclic Compounds. 2:521-525
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00477509
Popis:	The oxides of ethylene and propene, and epichlorohydrin, react with thionylanilines (ArN=S=O) in the presence of tetraethylammonium bromide catalyst at 95°–100° C to give N-arylalkeneamidosulfites, whose structures are confirmed by retrosynthesis from the corresponding N-phenylamino alcohols, and thionyl chloride, as well as by their IR spectra.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::8545abd1c30449dfb927ab736482dc9e https://doi.org/10.1007/bf00477509 Zobrazit plný text záznamu Full text from SpringerLink