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Synfacts 2010(6): 0654-0654
DOI: 10.1055/s-0029-1219985
DOI: 10.1055/s-0029-1219985
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag
Stuttgart ˙ New York
A Hyper-Reactive Tetrafluorinated Cumulene
C. Ehm, D. Lentz*
Freie Universität Berlin, Germany
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
20. Mai 2010 (online)
Significance
The authors report on the utility of the hyper-reactive tetrafluorobutatriene in the Diels-Alder reaction. Traditionally, this reagent has been very difficult to prepare and too unstable to use in reactions. Utilizing a recent, more efficient synthesis of the triene (A. Bach et al. Angew. Chem. Int. Ed. 2002, 41, 296), the authors were able to prepare the reagent and subsequently test the triene with a variety of dienes. In many reactions, conversion into the product is instantaneous and quantitative. The Diels-Alder products are stable to standard chromatographic work-up.