Iodocyclization of N, N-dialkylamino-2-methyl-4-penten-2-ol oxides

Autor:	V. I. Staninets, E. B. Koryak, Yu. I. Gevaza
Rok vydání:	1976
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Chemistry Group (periodic table) Organic Chemistry Iodide Intramolecular cyclization Oxide Organic chemistry Halogenation
Zdroj:	Chemistry of Heterocyclic Compounds. 12:1111-1114
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00945591
Popis:	It is shown that in the iodination of N,N-dialkylamino-2-methyl-4-penten-2-ol and N,N-diethylamino-3-butene oxides the N-oxide group participates in the intramolecular cyclization of these compounds. N,N-Dialkyl-4-methyl-4-hydroxy-6-iodomethyltetrahydro-1,2-oxazine iodides were obtained by iodination of the former, whereas the latter under similar conditions gives N,N-diethyl-5-iodomethyltetrahydro-1,2-oxazolinium iodide.
Databáze:	OpenAIRE
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