Hulme, A.N., McNab, H., Peggie, D.A. and Quye, A. (2005) Negative ion electrospray mass spectrometry of neoflavonoids. Phytochemistry, 66(23), pp. 2766-2770. (doi: 10.1016/j.phytochem.2005.09.001)
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Publisher's URL: http://dx.doi.org/10.1016/j.phytochem.2005.09.001
Abstract
The electrospray ionisation mass spectra of the neoflavanoids brazilin and hematoxylin are reported in both their reduced (1 and 2, respectively) and their oxidised forms (3 and 4, respectively). In the reduced forms, breakdown pathways under collision induced decomposition (CID) conditions produce fragments characteristic of rings A and C; in their oxidised forms, the fragments are characteristic of rings B and D. The structural assignments of the fragments are substantiated by recording the spectra after deuterium exchange at the hydroxyl groups.
Item Type: | Articles |
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Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | UNSPECIFIED |
Authors: | Hulme, A.N., McNab, H., Peggie, D.A., and Quye, A. |
Subjects: | Q Science > QD Chemistry |
College/School: | College of Science and Engineering > School of Chemistry |
Journal Name: | Phytochemistry |
ISSN: | 0031-9422 |
Published Online: | 20 October 2005 |
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