1970
DOI: 10.1016/s0031-9422(00)85235-8
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Hydrolysable tannins of Eucalyptus delegatensis wood

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Cited by 85 publications
(48 citation statements)
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“…The coupling constants of the sugar H-atoms were similar to those reported for isocorilagin [17]. Since J 1,2 (4.0 Hz) for HÀC (1) is larger for a-than for b-configured 1 C 4 -type tannins, the glucopyranose ring in 2 was assumed to adopt a skewed-boat geometry [18] [19].…”
supporting
confidence: 69%
“…The coupling constants of the sugar H-atoms were similar to those reported for isocorilagin [17]. Since J 1,2 (4.0 Hz) for HÀC (1) is larger for a-than for b-configured 1 C 4 -type tannins, the glucopyranose ring in 2 was assumed to adopt a skewed-boat geometry [18] [19].…”
supporting
confidence: 69%
“…Approximately 20 ellagitannins have been reported from the heartwood of Eucalyptus species (e.g. Seikel and Hillis, 1970;Hillis and Yazaki, 1973;Hart and Hillis, 1974;Yazaki et al, 1993). Other studies have noted the presence of numerous ellagitannins in eucalypt branch wood but have not identified individual compounds (Conde et al, 1995;Cadahia et al, 1997).…”
Section: Introductionmentioning
confidence: 99%
“…These two compounds were positively identified by comparison with authentic compounds (Table 3) (7) 112 (7), 239(100), 240(18), 241 (7), 254(83), 255 (17), 256 (7) 112 (12), 239(100), 240(15), 241 (7), 254(78), 255 (13) 133 (10), 239(100), 240 (18), 241 (7), 342(44), 343 (12) 239 (24), 342(100), 343(21), 344 (9) 133 (11) infected wood (Table 1). The extractive substances in normal oak probably consisted partially of phenoltype esters with glycosidic linkages to carbohydrate material (Seikel andHillis 1970, Scalbert et al 1988). The bacteria apparently were consuming the carbohydrate portion of the extractive substances and, in the process, were generating residues of resorcinol and pyrogallol.…”
Section: Gc-ms Resultsmentioning
confidence: 99%