The structures of the C-glycosidic ellagitannins, castalagin, vescalagin, casuarinin and stachyurin, have been revised to 1—4 respectively, on the basis of two-dimensional nuclear Overhauser effect (NOE) spectroscopy and NOE difference spectroscopy. Furthermore, the structures of some related C-glycosidic tannins were re-examined by using similar techniques, and it was concluded that the configuration at the glucose C-l position in all hitherto known C-glycosidic tannins must be revised. © 1990, The Pharmaceutical Society of Japan. All rights reserved.
CITATION STYLE
Nonaka, G. I., Sakai, T., Nishioka, I., & Mihashi, K. (1990). Tannins and Related Compounds: XCVII: Structure Revision of C-Glycosidic Ellagitannins, Castalagin, Vescalagin, Casuarinin and Stachyurin, and Related Hydrolyzable Tannins. Chemical and Pharmaceutical Bulletin, 38(8), 2151–2156. https://doi.org/10.1248/cpb.38.2151
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