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...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
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International Union of Crystallography
2010
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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. |
first_indexed | 2024-03-06T05:06:41Z |
format | Article |
id | um.eprints-1847 |
institution | Universiti Malaya |
language | English |
last_indexed | 2024-03-06T05:06:41Z |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | dspace |
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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