First synthesis of (±)-monotesone B and new syntheses of (±)-lonchocarpol A and (±)-bavachin

Ágnes Kenéz, Sándor Antus

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The first synthesis of (±)-monotesone B and new syntheses of (±)-lonchocarpol A and (±)-bavachin have been achieved starting from the corresponding MOM-protected C-prenylated acetophenone derivatives. Their antifungal activity was tested against Candida albicans.

Original languageEnglish
Pages (from-to)51-55
Number of pages5
JournalNatural Product Communications
Volume1
Issue number1
Publication statusPublished - 2006

Fingerprint

Candida albicans
synthesis
chemical derivatives
acetophenone
bavachin
senegalensin

Keywords

  • Antifungal activity
  • Bavachin
  • C-prenylated flavanones
  • Lonchocarpol A
  • Monotesone B
  • Synthesis

ASJC Scopus subject areas

  • Drug Discovery
  • Pharmacology
  • Complementary and alternative medicine
  • Plant Science

Cite this

First synthesis of (±)-monotesone B and new syntheses of (±)-lonchocarpol A and (±)-bavachin. / Kenéz, Ágnes; Antus, Sándor.

In: Natural Product Communications, Vol. 1, No. 1, 2006, p. 51-55.

Research output: Contribution to journalArticle

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