19 F NMR study of fluoro‐substituted tetracyclo[6.3.0.0 2,4 .0 3,7 ]undec‐5‐enes

19 F and 1 H NMR data are reported for fluoro‐substituted tetracyclo[6.3.0.0 2,4 .0 3,7 ]undec‐5‐enes, which are products of the meta photocycloaddition reaction of fluorobenzenes to cyclopentene. Hetero‐ and homo‐nuclear decoupling techniques were used to identify the adducts.

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Veröffentlicht in:Magnetic resonance in chemistry 1990-08, Vol.28 (8), p.722-728
Hauptverfasser: Osselton, E. M., Erkelens, C., Krijnen, E. S., Lempers, E. L. M., Cornelisse, J.
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Sprache:eng
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Zusammenfassung:19 F and 1 H NMR data are reported for fluoro‐substituted tetracyclo[6.3.0.0 2,4 .0 3,7 ]undec‐5‐enes, which are products of the meta photocycloaddition reaction of fluorobenzenes to cyclopentene. Hetero‐ and homo‐nuclear decoupling techniques were used to identify the adducts.
ISSN:0749-1581
1097-458X
DOI:10.1002/mrc.1260280812