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- W2326425992 abstract "The range of natural galloylhamameloses is extended by the recognition of the highly unstable novel analogues, the 1-O-(4-hydroxybenzoyl)-2′,5-di-O-galloyl-α-D-hamamelofuranose and its 1-O-β-anomer. The observed facile elimination of the C-1 acyl moiety is discussed and a mechanism proposed. These compounds are accompanied in the bark of Hamamelis virginiana by the “conventional” hamamelitannin, the related new 1,2′,5-tri-O-galloyl-α-D-hamamelofuranose, and a tentatively characterized di-O-galloyl-D-hamamelopyranose, the first pyranose analogue, shown to be also present in commercially available hamamelitannin. The structures of these compounds were established from spectroscopic evidence of their acetate derivatives." @default.
- W2326425992 created "2016-06-24" @default.
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- W2326425992 date "1994-10-01" @default.
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- W2326425992 title "Novel Galloylhamameloses from<i>Hamamelis virginiana</i><sup>1</sup>" @default.
- W2326425992 doi "https://doi.org/10.1055/s-2006-959533" @default.
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