Catalytic Codimerization of α,β- with γ,δ-Unsaturated Ketones: Novel Stereoselective Method of the Synthesis of Functionalized 8-Oxabicyclooctanes
Functionalized 8-oxabicyclooctanes (3a-e) were obtained in one stage from vinyl ketones and 5-methylhex-5-en-2-one or 1-phenyl-4-methylpenty-4-en-1-one in the presence of the catalytic system 2*SnCl2.
Kovalev, Igor P.,Ipatkin, Vyacheslav V.,Strelenko, Yury A.,Ignatenko, Anatoly V.,Nikishin, Gennady I.
Cycloaddition reaction with the participation of unsaturated ketones catalyzed by an Rh(I)-Sn(II) system
Codimerization of vinyl ketones with metallylacetone or metallylacetophenone in the presence of 2-SnCl2 affords substituted endo-2-acyl-8-oxabicyclooctanes, the products of the formal cycloaddition. - Key words: cycloaddition;
Strelenko, Yu. A.,Ipatkin, V. V.,Kovalev, I. P.,Nikishin, G. I.
p. 2187 - 2189
(2007/10/03)
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