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231224s2011 xx |||||o 00| ||eng c |
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|a 10.1002/mrc.2794
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|a eng
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|a Giordani, Raquel B
|e verfasserin
|4 aut
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|a Alkaloids from Hippeastrum morelianum Lem. (Amaryllidaceae)
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|c 2011
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|a Text
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Completed 04.05.2012
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|a Date Revised 20.09.2011
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2011 John Wiley & Sons, Ltd.
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|a The Amaryllidaceae family has proven to be a rich source of active molecules. As part of an ongoing project, we report a phytochemical study of Hippeastrum morelianum (Amaryllidaceae), from which we have isolated two homolycorine-type alkaloids, the new 2α,7-dimethoxyhomolycorine (1) and the poorly described candimine (2), as well as six known alkaloids: tazettine, pretazettine, 3-epimacronine, haemanthamine, hamayne and trisphaeridine. For reference purposes, the NMR of the isolated compounds was unequivocally described, based on 2D NMR measurements including (1)H-(1)H COSY, (1)H-(1)H NOESY, HSQC and HMBC
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|a Letter
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|a Research Support, Non-U.S. Gov't
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|a Alkaloids
|2 NLM
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|a Plant Extracts
|2 NLM
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|a de Andrade, Jean P
|e verfasserin
|4 aut
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|a Verli, Hugo
|e verfasserin
|4 aut
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|a Dutilh, Julie H
|e verfasserin
|4 aut
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|a Henriques, Amélia T
|e verfasserin
|4 aut
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|a Berkov, Strahil
|e verfasserin
|4 aut
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|a Bastida, Jaume
|e verfasserin
|4 aut
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|a Zuanazzi, José Angelo S
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 49(2011), 10 vom: 30. Okt., Seite 668-72
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
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|g volume:49
|g year:2011
|g number:10
|g day:30
|g month:10
|g pages:668-72
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