1,3,7-Trideacetyl-khivorin

Huaping Zhang; Don Vanderveer; Xi Wang; Feng Chen; Michael J. Wargovich

doi:10.1107/S1600536807055110

1,3,7-Trideacetyl-khivorin

Huaping Zhang, Don Vanderveer, Xi Wang, Feng Chen, Michael J. Wargovich

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

The title d-seco limonoid, named 1,3,7-trideacetyl-khivorin (systematic name: 14,15Β:21,23-diepoxy-1,3,7-trihydroxy-4,4,8-trimethyl-d-homo-24-nor- 17-oxochola-20,22-diene-16-one), C26H36O7, was isolated from the stem bark of African mahogany Khaya senegalensis (Meliaceae). The four fused six-membered rings adopt chair, chair, boat and half-chair conformations. The five-membered furan ring is disordered by a 180° rotation about the bond linking it to the pyran ring. The crystal structure is stabilized by strong classical O - H⋯O hydrogen-bond inter-actions to form a network.

Original language	English (US)
Pages (from-to)	o4599
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	63
Issue number	12
DOIs	https://doi.org/10.1107/S1600536807055110
State	Published - Nov 9 2007
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)
Materials Science(all)
Condensed Matter Physics

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title = "1,3,7-Trideacetyl-khivorin",

abstract = "The title d-seco limonoid, named 1,3,7-trideacetyl-khivorin (systematic name: 14,15Β:21,23-diepoxy-1,3,7-trihydroxy-4,4,8-trimethyl-d-homo-24-nor- 17-oxochola-20,22-diene-16-one), C26H36O7, was isolated from the stem bark of African mahogany Khaya senegalensis (Meliaceae). The four fused six-membered rings adopt chair, chair, boat and half-chair conformations. The five-membered furan ring is disordered by a 180° rotation about the bond linking it to the pyran ring. The crystal structure is stabilized by strong classical O - H⋯O hydrogen-bond inter-actions to form a network.",

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AU - Zhang, Huaping

AU - Vanderveer, Don

AU - Wang, Xi

AU - Chen, Feng

AU - Wargovich, Michael J.

PY - 2007/11/9

Y1 - 2007/11/9

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