(alpha R,4R,4aR,6aS,7R,8S,10R,11S)-Methyl alpha-acetoxy-4-(3-furanyl)-10-hydroxy-4a,7,9,9-tetramethyl-2,13-dioxo-1 ,4,4a,5,6,6a,7,8,9,10,11,12-dodecahydro-7,11-methano-2H-cycloocta[f] 2]benzopyran-8-acetate (6-O-acetylswietenolide) from the seeds of Swietenia macrophylla

Goh, B.H. and Kadir, H.A. and Malek, S.N.A. and Ng, S.W. (2010) (alpha R,4R,4aR,6aS,7R,8S,10R,11S)-Methyl alpha-acetoxy-4-(3-furanyl)-10-hydroxy-4a,7,9,9-tetramethyl-2,13-dioxo-1 ,4,4a,5,6,6a,7,8,9,10,11,12-dodecahydro-7,11-methano-2H-cycloocta[f] 2]benzopyran-8-acetate (6-O-acetylswietenolide) from the seeds of Swietenia macrophylla. Acta Crystallographica Section E: Structure Reports Online, 66 (11). O2802-U87. ISSN 1600-5368,

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Abstract

The molecule of O-acetylswietenolide, C29H36O9, isolated from the seeds of Swietenia macrophylla, features four six-membered rings connected together in the shape of a bowl; one of the inner rings adopts a twisted chair conformation owing to the C=C double bond. The furyl substitutent is connected to an outer ring, and it points away from the bowl cavity. The hydroxy group is connected to a carbonyl O atom of an adjacent molecule by an O-H center dot center dot center dot O hydrogen bond, generating a chain running along the b axis.

Item Type: Article
Funders: UNSPECIFIED
Subjects: Q Science > Q Science (General)
Depositing User: Mr Faizal 2
Date Deposited: 14 Jan 2015 01:59
Last Modified: 31 Jan 2019 04:11
URI: http://eprints.um.edu.my/id/eprint/12016

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