1-(4-Fluorobenzoyl)-9<i>H</i>-carbazole

Markus Laube; Jonas König; Martin Köckerling; Torsten Kniess

doi:10.3390/M1430

Molbank (Aug 2022)

1-(4-Fluorobenzoyl)-9<i>H</i>-carbazole

Markus Laube,
Jonas König,
Martin Köckerling,
Torsten Kniess

Affiliations

Markus Laube: Department Radiopharmaceutical and Chemical Biology, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, Bautzner Landstraße 400, 01328 Dresden, Germany
Jonas König: Department of Inorganic Solid-State Chemistry, Institute of Chemistry, University of Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany
Martin Köckerling: Department of Inorganic Solid-State Chemistry, Institute of Chemistry, University of Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany
Torsten Kniess: Department Radiopharmaceutical and Chemical Biology, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, Bautzner Landstraße 400, 01328 Dresden, Germany

DOI: https://doi.org/10.3390/M1430
Journal volume & issue: Vol. 2022, no. 3
p. M1430

Abstract

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1-(4-Fluorobenzoyl)-9H-carbazole (1) was synthesized, starting from 9H-carbazole and 4-fluorobenzonitrile, by Friedel–Crafts acylation, using boron trichloride to direct the substitution in 1-position. Single-crystal X-ray diffraction analysis unambiguously revealed the molecular structure of 1.

Published in Molbank

ISSN: 1422-8599 (Online)
Publisher: MDPI AG
Country of publisher: Switzerland
LCC subjects: Science: Chemistry: Inorganic chemistry
Website: https://www.mdpi.com/journal/molbank

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