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- W2783118860 endingPage "15564" @default.
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- W2783118860 abstract "Abstract In the long history of corannulene chemistry, the 1,3‐dipolar cycloaddition to corannulene is unprecedented. Reported herein is the 1,3‐dipolar cycloaddition of a polycyclic aromatic azomethine ylide to corannulene, a reaction which occurs exclusively at the rim bond of corannulene, from the convex side in an exo fashion. The cycloadducts were successfully converted, by successive oxidative dehydrogenation, into pyrrole‐fused corannulenes, which exhibited pronounced solvatofluorochromism." @default.
- W2783118860 created "2018-01-26" @default.
- W2783118860 creator A5028545567 @default.
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- W2783118860 date "2017-11-13" @default.
- W2783118860 modified "2023-10-18" @default.
- W2783118860 title "Synthesis of Pyrrole-Fused Corannulenes: 1,3-Dipolar Cycloaddition of Azomethine Ylides to Corannulene" @default.
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- W2783118860 doi "https://doi.org/10.1002/anie.201707087" @default.
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