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- W2952892575 abstract "In the presence of K 2 CO 3 and Et 3 N, pyridinium, quinolinium, isoquinolinium and benzimidazolinium N-ylides, generated in situ from their halides, react with gaseous flouroalkenes [CF 2 =CFX (1), X = Cl (a), Br (b), CF 3 (d)] in DMF under atmospheric pressure in normal glassware at 70 °C to give the corresponding fluorinated indolizines or H-pyrrolo[1,2-a]benzimidazoles via 1,3-dipolar [3+2] cycloaddition. Similar results are obtained with tetrafluoroethene in an autoclave." @default.
- W2952892575 created "2019-06-27" @default.
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- W2952892575 date "2003-04-15" @default.
- W2952892575 modified "2023-10-16" @default.
- W2952892575 title "Synthesis of Fluorinated Indolizines and 4H-Pyrrolo[1,2-a]benzimidazoles via 1,3-Dipolar Cycloaddition of Fluoroalkenes to N-Ylides." @default.
- W2952892575 doi "https://doi.org/10.1002/chin.200315150" @default.
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