22970-70-3Relevant articles and documents
REGIO- AND STEREOSELECTIVE OXYGENATION OF FLAVAN-3-OL-, 4-ARYLFLAVAN-3-OL-, AND BIFLAVANOID-DERIVATIVES WITH POTASSIUM PERSULPHATE
Mouton, C. Hendrik L.,Steenkamp, Jacobus A.,Young, Desmond A.,Bezuidenhoudt, Barend C. B.,Ferreira, Daneel
, p. 6885 - 6894 (2007/10/02)
The phenolic methyl ethers of flavan-3-ols, 4-arylflavan-3-ols, and (-)-fisetinidol-(4,8)-(+)-catechin biflavanoids are susceptible to regio- and stereoselective hydroxylation at C-4 in moderate to high yields with potassium persulphate/cupric sulphate in aqueous acetonitrile.The resultant 4-functionalized analogues are of both synthetic and degradative significance in condensed tannin chemistry.
Heterocycles. XVII. Sodium borohydride reduction of flavanonols and hydrolysis of (±)-fistacacidin acetates
Takahashi,Kubota,Iguchi,Onda
, p. 3134 - 3141 (2007/10/02)
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OCCURRENCE OF PROCYANIDINS IN NELIA MEYERI
Kolodziej, Herbert
, p. 1745 - 1752 (2007/10/02)
A novel natural 4-arylflavan-3-ol has been obtained from leaves of Nelia meyeri.The same extract contains two procyanidin dimers, B-2 and B-5, and trimer C-1. 1H NMR studies furnish diagnostic chemical shift parameters for determining the points of linkag