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Acta Cryst. (2003). E59, o347-o349  [ doi:10.1107/S1600536803003374 ]

The acetyl derivative of humirianthol

R. A. Burrow, A. F. Morel, I. B. Graebner, D. H. Farrar and A. J. Lough

Abstract: The title compound, 15[alpha]-acetato-3[beta],20:14[beta],16-diepoxy-3[alpha]-hydroxy-9-epi-7-pimaren-19,6[beta]-olide, C22H28O7, formed from the acetylation of humirianthol, isolated from the tubers of Humirianthera ampla, crystallizes in the chiral space group P212121. The absolute configuration was set using the absolute configuration of C15, as determined by the Horeau method. The structure comprises a pimarane ring system with a methylene ether bridge over ring A, a double bond in ring B, and two five-membered furanyl rings, one fused to rings A and B and the other to ring C.

Online 21 February 2003


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