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Search for "malassezione" in Full Text gives 1 result(s) in Beilstein Journal of Organic Chemistry.

Convenient alternative synthesis of the Malassezia-derived virulence factor malassezione and related compounds

  • Karu Ramesh and
  • Stephen L. Bearne

Beilstein J. Org. Chem. 2025, 21, 1730–1736, doi:10.3762/bjoc.21.135

Graphical Abstract
  • are commensal fungi that constitute the normal skin microbiota but may become pathogenic. These fungi, especially M. furfur, convert tryptophan into various alkaloid indoles such as malassezione, which may serve as virulence factors. To facilitate testing of malassezione as an aryl hydrocarbon
  • -protected malassezione, which upon deprotection yields malassezione in an overall yield of ca. 20%. This is an improvement over the preparation of the isonitrile followed by an Fe hydride initiated isonitrile–olefin intramolecular coupling reaction, which generated malassezione with an overall yield of ca
  • . 5%. Furthermore, the present method may also be used to prepare related compounds. Keywords: bis(aryl/heteroaryl)ketones; EDC; indole alkaloids; malassezione; Introduction Lipophilic yeasts of the genus Malassezia are commensal fungi that constitute the normal skin microbiota; however, when they
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Published 28 Aug 2025
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