Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings
The bark extract of the Malayan Alstonia angustifoliaWall provided the spirocyclic alkaloids macrodasines A—G. The structures of the new compounds were established by analysis of the spectroscopic data and in the case of macrodasines A and B confirmed by X-ray diffraction analysis. Macrodasines A, B...
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2011
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my.um.eprints.103922014-10-15T01:51:46Z http://eprints.um.edu.my/10392/ Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings Kam, T.S. Tan, S.J. Robinson, W.T. Komiyama, K. QD Chemistry The bark extract of the Malayan Alstonia angustifoliaWall provided the spirocyclic alkaloids macrodasines A—G. The structures of the new compounds were established by analysis of the spectroscopic data and in the case of macrodasines A and B confirmed by X-ray diffraction analysis. Macrodasines A, B, C, and G incorporate fused spirocyclic tetrahydrofuran—tetrahydrofuran rings, while macrodasines D, E, and F incorporate fused tetrahydrofuran—tetrahydropyran rings. Macrodasines B, C, and E were found to show moderate levels of activity in reversing multidrug-resistance in drug-resistant KB cells. Elsevier 2011 Article PeerReviewed application/pdf en http://eprints.um.edu.my/10392/1/Macrodasines_A%E2%80%94G%2C_macroline_indole_alkaloids_incorporating_fused_spirocyclic_tetrahydrofuran%E2%80%94tetrahydrofuran_and_tetrahydrofuran%E2%80%94tetrahydropyran_rings.pdf Kam, T.S. and Tan, S.J. and Robinson, W.T. and Komiyama, K. (2011) Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings. Tetrahedron, 67. pp. 3830-3838. ISSN 0040-4020 doi:10.1016/j.tet.2011.03.099 |
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QD Chemistry Kam, T.S. Tan, S.J. Robinson, W.T. Komiyama, K. Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
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The bark extract of the Malayan Alstonia angustifoliaWall provided the spirocyclic alkaloids macrodasines A—G. The structures of the new compounds were established by analysis of the spectroscopic data and in the case of macrodasines A and B confirmed by X-ray diffraction analysis. Macrodasines A, B, C, and G incorporate fused spirocyclic tetrahydrofuran—tetrahydrofuran rings, while macrodasines D, E, and F incorporate fused tetrahydrofuran—tetrahydropyran rings. Macrodasines B, C, and E were found to show moderate levels of activity in reversing multidrug-resistance in drug-resistant KB cells. |
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Article |
author |
Kam, T.S. Tan, S.J. Robinson, W.T. Komiyama, K. |
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Kam, T.S. Tan, S.J. Robinson, W.T. Komiyama, K. |
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Kam, T.S. |
title |
Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
title_short |
Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
title_full |
Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
title_fullStr |
Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
title_full_unstemmed |
Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
title_sort |
macrodasines a—g, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings |
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Elsevier |
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2011 |
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http://eprints.um.edu.my/10392/1/Macrodasines_A%E2%80%94G%2C_macroline_indole_alkaloids_incorporating_fused_spirocyclic_tetrahydrofuran%E2%80%94tetrahydrofuran_and_tetrahydrofuran%E2%80%94tetrahydropyran_rings.pdf http://eprints.um.edu.my/10392/ |
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