SYNTHESIS OF ENYNES ON THE BASIS OF 2-METHYL-HEPTENE-6-YN-3-OL-2
A.M.Garamanov, M.G.Veliev, S.N.Allakhverdieva, S.S.Hasanova, A.F.Gulieva
The diene synthesis reaction of 2-methyl-heptene-6-yn-3-ol-2 and its some functionally substituted derivatives with hexachloro- and 5,5-dimetoxytetrachlorcyclopentadienes in a medium of p-xylol at 125–130°C has been investigated. It has been shown that the reaction proceeds due to end double bond with formation of endo-adducts. A yield is 80–90%.
Keywords : 2-methyl-heptene-6-yn-3-ol-2, hexachlorocyclopentadiene, 5,5-dimethoxytetrachlorocyclopentadiene, p-xylol, diene synthesis, endo-adduct
View article
SUBMITION
THE LAST NUMBER OF THE JOURNAL
№3 2026CONTENT
- STUDY OF THE PROCESS OF ELECTROREDUCTION OF ANTIMONY IONS FROM AN ACIDIC ELECTROLYTEN.A. Aliyeva Mammadova, S.F. Jafarova, S.P. Javadova, Sh.A. Ibrahimova, A.A. Aliyev, S.D. Dadashova, M.F. Nabiyeva, M.T.Abbasov, H.Ch. Aliyeva, D.B. Tagiyev- WATERMELON RIND ADSORBENT FOR ATTENUATION OF HEAVY METAL CONTAMINATED WATER: GAUSSIAN PROCESS REGRESSION FOR RSM OPTIMIZATIONM. Abubakar, Y. A. Musti, I. U. Usman, W. C. Ulakpa, A. M. Abubakar, M. Al-HedrewyMore
.png)