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- W888932432 abstract "The authors have studied the Diels-Alder reactions between furan derivatives and maleimide derivatives in an ionic liquid and have found that higher reactivity can be obtained in a protic ionic liquid [Mim]Tf2N than in the conventional organic solvent. Furthermore, in the Diels-Alder reactions of 2- and 2,5-alkylfurans with N-alkylma-leimide, the reactivity increases by extending the alkyl chain length of N-alkylmaleimide. In addition, it was demon-strated that endo-selectivity increases when 2,5-disubstituted furans are used. These results will be explained by comparing the stability of the Diels-Alder adduct with that of the products obtained from the reactions of 2-substituted furans and 2,5-disubstituted furans." @default.
- W888932432 created "2016-06-24" @default.
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- W888932432 date "2009-01-01" @default.
- W888932432 modified "2023-09-25" @default.
- W888932432 title "Furans-Maleimides Diels-Alder Reactions in Protic Ionic Liquid" @default.
- W888932432 hasPublicationYear "2009" @default.
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