Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor
A new monoterpene indole alkaloid characterized by an unprecedented pentacyclic cage skeleton, arboridinine (1), was isolated from a Malaysian Kopsia species. The structure and absolute configuration of the alkaloid were determined based on NMR, MS, and X-ray diffraction analysis. A possible biogene...
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my.um.eprints.194432018-09-28T02:17:44Z http://eprints.um.edu.my/19443/ Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor Wong, S.P. Gan, C.Y. Lim, K.H. Ting, K.N. Low, Y.Y. Kam, T.S. Q Science (General) QA75 Electronic computers. Computer science QD Chemistry R Medicine TA Engineering (General). Civil engineering (General) A new monoterpene indole alkaloid characterized by an unprecedented pentacyclic cage skeleton, arboridinine (1), was isolated from a Malaysian Kopsia species. The structure and absolute configuration of the alkaloid were determined based on NMR, MS, and X-ray diffraction analysis. A possible biogenetic pathway from a pericine precursor is presented. American Chemical Society 2015 Article PeerReviewed Wong, S.P. and Gan, C.Y. and Lim, K.H. and Ting, K.N. and Low, Y.Y. and Kam, T.S. (2015) Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor. Organic Letters, 17 (14). pp. 3628-3631. ISSN 1523-7060 http://dx.doi.org/10.1021/acs.orglett.5b01757 doi:10.1021/acs.orglett.5b01757 |
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Q Science (General) QA75 Electronic computers. Computer science QD Chemistry R Medicine TA Engineering (General). Civil engineering (General) Wong, S.P. Gan, C.Y. Lim, K.H. Ting, K.N. Low, Y.Y. Kam, T.S. Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor |
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A new monoterpene indole alkaloid characterized by an unprecedented pentacyclic cage skeleton, arboridinine (1), was isolated from a Malaysian Kopsia species. The structure and absolute configuration of the alkaloid were determined based on NMR, MS, and X-ray diffraction analysis. A possible biogenetic pathway from a pericine precursor is presented. |
format |
Article |
author |
Wong, S.P. Gan, C.Y. Lim, K.H. Ting, K.N. Low, Y.Y. Kam, T.S. |
author_facet |
Wong, S.P. Gan, C.Y. Lim, K.H. Ting, K.N. Low, Y.Y. Kam, T.S. |
author_sort |
Wong, S.P. |
title |
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor |
title_short |
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor |
title_full |
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor |
title_fullStr |
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor |
title_full_unstemmed |
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor |
title_sort |
arboridinine, a pentacyclic indole alkaloid with a new cage carbon–nitrogen skeleton derived from a pericine precursor |
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American Chemical Society |
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2015 |
url |
http://eprints.um.edu.my/19443/ http://dx.doi.org/10.1021/acs.orglett.5b01757 |
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1643690990040514560 |