Molecules (Feb 2002)

Photooxygenation of Nimonol, a Tetranortriterpenoid from Azadirachta indica. A. Juss.

  • V. Kasinath,
  • N. D. Pradeep Singh,
  • Geetha Gopalakrishnan

DOI
https://doi.org/10.3390/70200112
Journal volume & issue
Vol. 7, no. 2
pp. 112 – 118

Abstract

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Nimonol (1), a tetranortriterpenoid isolated from the leaves of Azadirachta indica A. Juss (Meliaceae), upon photolysis undergoes both Diels-Alder and ene reactions with singlet oxygen at different sites leading to 14,15,20,21-diepoxy-23-nimonolactone (3), along with nimonolide (4), which have been well-characterised. The novelty of the reported reactions lies in hitherto unreported formation of an α-epoxide in the ring D in tetranortriterpenoids. The photoproduct 4 exhibited antifeedancy comparable to that of azadirachtin-A, the most potent antifeedant constituent isolated from neem.

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