104263-86-7Relevant articles and documents
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Robertson
, p. 1946,1951 (1959)
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A-type proanthocyanidins from peanut skins
Lou, Hongxiang,Yamazaki, Yoshimitsu,Sasaki, Tsutomu,Uchida, Masaru,Tanaka, Hideoki,Oka, Syuichi
, p. 297 - 308 (2007/10/03)
Six A-type proanthocyanidins were isolated from the water-soluble fraction of peanut skins. On the basis of spectral data, reductive cleavage with sodium cyanoborohydride, and chiral HPLC analysis, three new compounds, epicatechin-(2β → O → 7, 4β → 6)-catechin, epicatechin-(2β → O → 7, 4β → 6)-ent-catechin and epicatechin-(2β → O → 7, 4β → 6)-ent- epicatechin were unambiguously identified, together with the three known compounds, proanthocyanidin A-1, proanthocyanidin A-2 and epicatechin-(2β → O → 7, 4β → 8)-ent-epicatechin. 13C NMR chemical shift rules to distinguish between [2 → O → 7, 4 → 8] and [2 → O → 7,4 → 6] double- linked heptamethyl ethers of A-type proanthocyanidins are proposed. Bioassay experiments showed that these six compounds possess substantial activity against hyaluronidase.
Proton magnetic resonance spectra of catechin and bromocatechin derivatives: C6- vs. C8-substitution
Kiehlmann, E.,Tracey, A. S.
, p. 1998 - 2005 (2007/10/02)
The 1Hmr spectra of 20 catechin derivatives substituted at C-6/C-8 by bromine and/or hydrogen and at oxygen by methyl, acetyl, and/or hydrogen have been analyzed in deuterated acetone, acetonitrile, and chloroform.Because of its dependence on the nature o
