Swietenolide diacetate from the seeds of Swietenia macrophylla

The title compound, C31H38O10 [systematic name: (�R,4R,4aR,6aS,7R,8S,10R,11S)-methyl �,10-diacetoxy-4-(3- furyl)-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], was isolated from the seeds of Swietenia macrophylla. Th...

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Main Authors: Goh, B.H., Abdul Kadir, H., Abdul Malek, S.N., Ng, S.W.
Format: Article
Language:English
Published: International Union of Crystallography 2010
Subjects:
Online Access:http://eprints.um.edu.my/1847/1/Swietenolide_diacetate_from_the_seeds_of_Swietenia_macrophylla.pdf
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author Goh, B.H.
Abdul Kadir, H.
Abdul Malek, S.N.
Ng, S.W.
author_facet Goh, B.H.
Abdul Kadir, H.
Abdul Malek, S.N.
Ng, S.W.
author_sort Goh, B.H.
collection UM
description The title compound, C31H38O10 [systematic name: (�R,4R,4aR,6aS,7R,8S,10R,11S)-methyl �,10-diacetoxy-4-(3- furyl)-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], was isolated from the seeds of Swietenia macrophylla. The molecule contains 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 carbon–carbon double bond. The furyl substitutent is connected to an outer ring, and it points away from the bowl cavity.
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spelling um.eprints-18472019-01-31T08:36:05Z http://eprints.um.edu.my/1847/ Swietenolide diacetate from the seeds of Swietenia macrophylla Goh, B.H. Abdul Kadir, H. Abdul Malek, S.N. Ng, S.W. QD Chemistry The title compound, C31H38O10 [systematic name: (�R,4R,4aR,6aS,7R,8S,10R,11S)-methyl �,10-diacetoxy-4-(3- furyl)-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], was isolated from the seeds of Swietenia macrophylla. The molecule contains 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 carbon–carbon double bond. The furyl substitutent is connected to an outer ring, and it points away from the bowl cavity. International Union of Crystallography 2010 Article PeerReviewed application/pdf en http://eprints.um.edu.my/1847/1/Swietenolide_diacetate_from_the_seeds_of_Swietenia_macrophylla.pdf Goh, B.H. and Abdul Kadir, H. and Abdul Malek, S.N. and Ng, S.W. (2010) Swietenolide diacetate from the seeds of Swietenia macrophylla. Acta Crystallographica Section E: Structure Reports Online, 66 (6). o1396-o1396. ISSN 1600-5368, DOI https://doi.org/10.1107/S1600536810017733 <https://doi.org/10.1107/S1600536810017733>. http://dx.doi.org/10.1107/S1600536810017733 doi:10.1107/S1600536810017733
spellingShingle QD Chemistry
Goh, B.H.
Abdul Kadir, H.
Abdul Malek, S.N.
Ng, S.W.
Swietenolide diacetate from the seeds of Swietenia macrophylla
title Swietenolide diacetate from the seeds of Swietenia macrophylla
title_full Swietenolide diacetate from the seeds of Swietenia macrophylla
title_fullStr Swietenolide diacetate from the seeds of Swietenia macrophylla
title_full_unstemmed Swietenolide diacetate from the seeds of Swietenia macrophylla
title_short Swietenolide diacetate from the seeds of Swietenia macrophylla
title_sort swietenolide diacetate from the seeds of swietenia macrophylla
topic QD Chemistry
url http://eprints.um.edu.my/1847/1/Swietenolide_diacetate_from_the_seeds_of_Swietenia_macrophylla.pdf
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