1H and 13C NMR assignments of two new isomeric bisbenzylisoquinoline alkaloids from Cissampelos sympodialis Eichl. (Menispermaceae)
des‐7′‐O‐methylroraimine (compound 1) and epi‐des‐7′‐O‐methylroraimine (compound 2), two new isomeric bisbenzylisoquinoline alkaloids were isolated and characterized as a mixture from the rhizomes of Cissampelos sympodialis Eichl. The unambiguous structural elucidation of both isomers was performed...
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Veröffentlicht in: | Magnetic resonance in chemistry 2013-05, Vol.51 (5), p.312-315 |
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Sprache: | eng |
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Zusammenfassung: | des‐7′‐O‐methylroraimine (compound 1) and epi‐des‐7′‐O‐methylroraimine (compound 2), two new isomeric bisbenzylisoquinoline alkaloids were isolated and characterized as a mixture from the rhizomes of Cissampelos sympodialis Eichl. The unambiguous structural elucidation of both isomers was performed with the aid of HR‐ESI‐MS, FT‐IR, and NMR techniques including COSY, HMQC, HMBC, and NOESY. Copyright © 2013 John Wiley & Sons, Ltd.
des‐7′‐O‐methylroraimine (1) and epi‐des‐7′‐O‐methylroraimine (2), two new isomeric bisbenzylisoquinoline alkaloids were isolated and characterized as a mixture from the rhizomes of Cissampelos sympodialis Eichl. The unambiguous structural elucidation of both isomers was performed with the aid of HR‐ESI‐MS, FT‐IR, and NMR techniques including COSY, HMQC, HMBC, and NOESY. |
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ISSN: | 0749-1581 1097-458X |
DOI: | 10.1002/mrc.3941 |