POLYBROMOCYCLOPENTADIENES IN THE DIENE SYNTHESIS REACTION. VII. RAECTIVITY OF HEXABROMO-1,3-CYCLOPENTADIENE IN THE DIENE SYNTHESIS REACTION WITH ARYL ACRYLATES
The reactivity of hexabromo-1,3-cyclopentadiene in the diene synthesis reaction with arylacrylates was studied.It was shown that the reaction is promoted by electron-donating and electron-withdrawing substituents in the aromatic ring.The view is expressed that the investigated diene-dienophile system reacts by a mechanism of the "neutral" type of diene synthesis.
Mustafaev, A. M.,Imamaliev, A. B.,Guseinov, M. M.
p. 1314 - 1317
(2007/10/02)
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