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- W2950607483 abstract "The 3H-pyrroles (I) react with N-phenylmaleimide (II) in benzene, at room temp. or under reflux, to give the endo Diels-Alder adducts (III); the adducts (IV) are similarly obtained." @default.
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- W2950607483 date "1990-01-09" @default.
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- W2950607483 title "ChemInform Abstract: The Synthesis and Chemistry of Azolenines. Part 14. The Combination of 3H- and 2H-Pyrroles with N-Phenylmaleimide: Diels-Alder Reactions and Michael Additions." @default.
- W2950607483 doi "https://doi.org/10.1002/chin.199002169" @default.
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