Inter- and intramolecular rearrangements of cyanuric acid triallyl esters

Autor:	V. R. Likhterov, E. G. Pomerantseva, V. S. Etlis, S. V. Klenovich, S. M. Shmuilovich, L. A. Tsareva
Rok vydání:	1988
Předmět:	chemistry.chemical_compound Chemistry Intramolecular force Organic Chemistry Organic chemistry Ether Cyanuric acid Catalysis Isocyanuric acid
Zdroj:	Chemistry of Heterocyclic Compounds. 24:308-311
ISSN:	1573-8353 0009-3122
Popis:	It is shown that the catalytic and thermal rearrangements of cyanuric acid triallyl esters to isocyanuric acid esters proceed via inter- and intramolecular mechanisms. Cross-reaction products are formed when the reaction is carried out with a mixture of homologs, while the reaction in the presence of a hydroxy-containing compound gives its allyl ether and diallyl isocyanurate.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ef5a0bb16a04f83793bd27e673f85853 https://doi.org/10.1007/bf00475330 Zobrazit plný text záznamu Full text from SpringerLink