

Author: Sun Wenxiu
Publisher: Taylor & Francis Ltd
ISSN: 1478-6419
Source: Natural Product Research, Vol.23, Iss.10, 2009-10, pp. : 960-962
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Lappaconitine is an important alkaloid of the aconite family and its biological activity is closely related to its structure. Through an X-ray structure analysis of hydrated lappaconitine hydrobromide, which was synthesised by us through a new method, the absolute configuration of lappaconitine was determined: monoclinic, P21, a = 10.619(2) Å, b = 12.196(3) Å, c = 12.282(2) Å, β = 90.87(1)° and Z = 2; Flack parameter is -0.0083(0.0046) and S = 0.867. Rings A, B, C, D, E and F, respectively, present boat, chair, envelope, boat, boat and envelope forms. The absolute stereo configuration of lappaconitine was determined as 1S, 4S, 5S, 7S, 8S, 9S, 10S, 11S, 13R, 14S, 16S and 17R.
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