INTER- AND INTRAMOLECULAR REARRANGEMENTS OF CYANURIC ACID TRIALLYL ESTERS
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.
Likhterov, V. R.,Klenovich, S. V.,Etlis, V. S.,Tsareva, L. A.,Pomerantseva, E. G.,Shmuilovich, S. M.
p. 308 - 311
(2007/10/02)
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