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- W2951874580 abstract "The dipolar cycloaddition of carbonyl ylides generated by the rhodium-catalyzed decomposition of δ- and ε-carbonyl-α-diazoketones with p-quinones leads to both CO and CC addition products. The product ratio is solvent- and catalyst-dependent and has been optimized to favor formation of either product. The CC addition products of naphthoquinones are used in the assembly of structures hybridizing the illudin and anthraquinone anticancer agents." @default.
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- W2951874580 date "2000-01-11" @default.
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- W2951874580 title "Dipolar Cycloaddition of Rhodium-Generated Carbonyl Ylides with <i>p</i>-Quinones" @default.
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- W2951874580 doi "https://doi.org/10.1021/ol991300s" @default.
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