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• W2056076911 abstract "A palladium-catalysed four-component process is described involving carbon monoxide, allene and aryl/heteroaryl iodides generating (π-allyl) palladium species, which are intercepted by alkene tethered nitrogen nucleophiles to afford 1,6- and 1,7-dienones. Subsequent ring closing metathesis affords five- and six-membered N-heterocyclic enones. The N-heterocyclic enones are active dipolarophiles in 1,3-dipolar cycloaddition reactions as exemplified by azomethine ylide and nitrone cycloadditions." @default.
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• W2056076911 date "2005-11-01" @default.
• W2056076911 modified "2023-10-09" @default.
• W2056076911 title "Four-component Pd-catalysed cascade/ring closing metathesis. Synthesis of heterocyclic enones" @default.
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• W2056076911 doi "https://doi.org/10.1016/j.tet.2005.09.015" @default.
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