Enantioselective Alkynylation of some Cyclical Ketones by 3,3′-Diphenylbinaphtol Dilithium

  • G.Q.Otamukhamedova, O.E.Ziyadullayev, A.Ikramov

Abstract

Process of enantioselective alkynylation of some cyclical ketones – cyclohexanon,
2-methylcyclohexanon, menton and camphora by 3,3′-diphenylbinaphtol dilithium has been investigated and mechanism of it’s carring out has been proposed. Influence of quantity of catalyst on the yield of product was investigated. Purity and structure of synthesised alcohols such as 1-(2-phenylethynil) cyclohexanol, 2-methyl-1-(2-phenylethynil) cyclohexanol, 2-isopropyl-5-methyl-1-(2-phenylethynil) cyclohexanol and 1,7,7-threemethyl-2-(2-phenylethynil) biciclo
[2,2,1]-heptanol-2 have been determined by different physico-chemical methods.

Published
2020-06-04
How to Cite
G.Q.Otamukhamedova, O.E.Ziyadullayev, A.Ikramov. (2020). Enantioselective Alkynylation of some Cyclical Ketones by 3,3′-Diphenylbinaphtol Dilithium. International Journal of Advanced Science and Technology, 29(12s), 2503-2511. Retrieved from http://sersc.org/journals/index.php/IJAST/article/view/24727
Section
Articles