%0 Journal Article 
%A Núñez Ventura, Araceli
%A Cuadro Palacios, Ana María
%A Álvarez-Builla Gómez, Julio
%A Vaquero López, Juan J.
%T Enyne ring-closing metathesis on heteroaromatic cations
%D 2006
%@ 1359-7345
%U http://hdl.handle.net/10017/3215
%X Cationic heteroaromatic enynes have been employed as substrates in enyne ring-closing metathesis, under an atmosphere of ethylene and using the Hoveyda-Grubbs catalyst, for the first time; the reaction affords new 1-vinyl- and 2-vinyl-substituted 3,4-dihydroquinolizinium salts, useful precursors for biologically relevant cations based on the quinolinizium system.
%K 1 Vinyl 3,4 dihydroquinolizinium derivative
%K 2 Vinyl 3,4 dihydroquinolizinium derivative
%K Berberine derivative
%K Cation
%K Coralyne
%K Dihydroquinoline derivative
%K Enyne derivative
%K Ethylene
%K Heteroaromatic cation
%K Unclassified drug
%K Article
%K Cation transport
%K Chemical structure
%K Product recovery
%K Ring closing metathesis
%K Structure activity relation
%K Structure analysis
%K Ciencia
%K Química orgánica
%K Science
%K Chemistry, organic
%~ Biblioteca Universidad de Alcala