Acta Cryst. (2005). E61, o2743-o2745  [ doi:10.1107/S1600536805023378 ]

Redetermination of 14-deoxyandrographolide

K. Bhattacharyya, T. Kar, G. Bocelli, A. Cantoni, S. Pramanick, S. Banerjee and S. Mukhopadhyay

Abstract: The title compound [systematic name: ent-3-hydroxy-8(17),13(14)-labdadiene-16,15-olide], C₂₀H₃₀O₄, contains two trans fused six-membered rings, with a lactone ring at the end of an equatorial side chain. The six-membered rings are in chair conformations and the lactone ring is planar. There is an infinite chain of both inter- and intramolecular O-HO hydrogen bonds along the b axis. The present study is a confirmation of the results of previous structure determinations of 14-deoxyandrographolide by Medforth, Chang, Chen, Olmstead & Smith [J. Chem. Soc. Perkin Trans. 2 (1990), pp. 1011--1016] and Rajnikant, Gupta, Singh, Lal, Gupta & Varghese [Mol. Cryst. Liq. Cryst. Sect. C (1996), 6, 227-233].

Online 30 July 2005

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