Química Nova (Jun 1997)

Determinação da Estereoquímica Relativa de Pimaradienos Através de Produtos de Oxidação Relative stereochemistry determination of pimaradienes through oxidative products

  • Frederico Guaré Cruz,
  • Nídia Franca Roque

DOI
https://doi.org/10.1590/S0100-40421997000300006
Journal volume & issue
Vol. 20, no. 3
pp. 261 – 266

Abstract

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Pimaradienes, including isopimaradienes, with an endocyclic double bond between C-9 and C-11 are uncommon compounds in nature. The diterpenoid pimar-9(11),15-dien-19-oic acid (1) was isolated from Mikania triangularis (Asteraceae) and the correct stereochemistry of 1was established by ¹H and 13C NMR studies of several oxidative products, mainly epoxides, of this compound and its double bond isomers.

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