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- W2004002411 abstract "[reaction: see text]. A series of quinone monoacetals bearing electron-withdrawing groups was treated with diethyl malonate and other bifunctional nucleophiles in the presence of KO-t-Bu in THF. Reactions of ethyl 3-nitropropionate or diethyl malonate resulted in single conjugate addition adducts. When ethyl acetoacetate was used as a nucleophile, bridged bicyclic products were obtained in good yields. The regiochemistry of conjugate addition was dependent on the quinone monoacetal substitution." @default.
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- W2004002411 date "2005-06-24" @default.
- W2004002411 modified "2023-09-27" @default.
- W2004002411 title "Regioselective Single and Double Conjugate Additions to Substituted Cyclohexa-2,5-dienone Monoacetals" @default.
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- W2004002411 doi "https://doi.org/10.1021/ol050715c" @default.
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