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- W2022355692 abstract "3-(2H-Pyran-2-on-6-yl)indolizines 6a-d were prepared by 1,3-dipolar cycloaddition reactions of N-(2H-pyran-2-on-6-yl)methylpyridinium bromides 5a,b with dimethyl acetylenedicarboxylate (DMAD). All of the cycloaddition reactions of 6b with N-phenylmaleimide, p-benzoquinone, and DMAD took place at the 2-pyrone ring to give 3-substituted indolizines." @default.
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- W2022355692 date "2010-08-22" @default.
- W2022355692 modified "2023-09-25" @default.
- W2022355692 title "ChemInform Abstract: Preparation of 3-(2H-Pyran-2-on-6-yl)indolizines and the Diels-Alder Reactions with Some Olefinic and Acetylenic Dienophiles." @default.
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- W2022355692 doi "https://doi.org/10.1002/chin.199219203" @default.
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