Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 25, Pages 2690-2692Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b602420c
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Cationic heteroaromatic enynes have been employed as substrates in enyne ring-closing metathesis, under an atmosphere of ethylene and using theHoveyda - 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.
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