37064-31-6Relevant academic research and scientific papers
Oxidation of Procyanidins with Various Degrees of Condensation: Influence on the Color-Deepening Phenomenon
Hibi, Yoshihide,Yanase, Emiko
, (2019)
Color deepening in red rice is a known phenomenon that occurs during postharvest storage. As procyanidins potentially causes this color deepening, we previously subjected synthetic procyanidin B3, a model procyanidin, to chemical oxidation and determined the structures of the products. To further elucidate the effects of various degrees of polymerization on color deepening, in this study we oxidized synthetic procyanidin C2. The intensity of the UV-vis absorption between 300 and 500 nm in the spectrum of the reaction mixture increased with increasing oxidation time. This absorption following the oxidation of procyanidin C2 was more intense than that of procyanidin B3. HPLC-ESI-MS of the oxidized reaction mixture revealed several new peaks that suggested the formation of products with new intramolecular rather than intermolecular bonds. The major product was structurally identified by comparison with the UPLC-ESI-MS/MS data for a synthetic procyanidin C2 oxide, independently prepared by condensing procyanidin B3 oxide and taxifolin.
Synthesis of procyanidins C2 and C1 using lewis acid mediated equimolar condensation
Oizumi, Yukiko,Katoh, Miyuki,Makabe, Hidefumi,Hattori, Yasunao,Toda, Kazuya,Kawaguchi, Koichiro,Fujii, Hiroshi
, p. 2241 - 2250,10 (2020/08/31)
Synthesis of procyanidins C2 and C1 was achieved via a stereoselective intermolecular condensation of equimolar amount of dimeric catechin or epicatechin nucleophile and monomeric catechin or epicatechin electrophile using Lewis acid. In the case of synthesis of procyanidin C2, AgBF4 and AgOTf afforded condensed product in excellent yield. As to the synthesis of procyanidin C1, Yb(OTf)3 was effective for equimolar condensation.
Efficient stereoselective synthesis of proanthocyanidin trimers with TMSOTf-catalyzed intermolecular condensation
Saito, Akiko,Tanaka, Akira,Ubukata, Makoto,Nakajima, Noriyuki
, p. 1069 - 1073 (2007/10/03)
A stereoselective synthesis of seven benzylated proanthocyanidin trimers with TMSOTf-catalyzed condensation reaction is described. In particular, epicatechin-(4β-8)-epicatechin-(4β-8)-epicatechin trimer (procyanidin C1), catechin-(4α-8)-catechin-(4α-8)-catechin trimer (procyanidin C2), epicatechin-(4β-8)-epicatechin-(4?-8)-catechin trimer and epicatechin-(4?-8)-catechin-(4α-8)-epicatechin trimer derivatives were obtained in excellent yields. The structure of benzylated procyanidin C2 was confirmed by comparing the 1H NMR spectra of protected procyanidin C2 that was synthesized by two different condensation approaches. Finally, deprotection of (+)-catechin and (-)-epicatechin trimers derivatives gave four natural procyanidin trimers in good yields.
Oligomeric flavanoids. Part 27. Interflavanyl bond formation in procyanidins under neutral conditions
Steynberg, Petrus J.,Nel, Reinier J.J.,Van Rensburg, Hendrik,Bezuidenhoudt, Barend C.B.,Ferreira, Daneel
, p. 8153 - 8158 (2007/10/03)
Dimethyl(methylthio)sulfonium tetrafluoroborate (DMTSF) and silver tetrafluoroborate (AgBF4) activate the C4-S bond in the 4-thioethers of flavan-3-ols toward carbon nucleophiles to permit formation of the interflavanyl bond in procyanidins under neutral conditions.
Extensive High-Resolution Reverse 2D NMR Analysis for the Structural Elucidation of Procyanidin Oligomers
Balas, Laurence,Vercauteren, Joseph
, p. 386 - 393 (2007/10/02)
The structures of the procyanidin dimers catechin-(4α-8)-catechin and catechin-(4α-6)-catechin were proved by spectroscopic means.To distinguish between the two possible interflavonoid linkages, it is necessary to assign all the quaternary aromatic carbon signals.How these assignments can be made through two-dimensional NMR spectroscopy is described. - Keywords: 2D NMR 1H NMR 13C NMR Structural analysis Proanthocyanidins Catechin dimers Tannins
SYNTHESIS AND CHARACTERIZATION OF PROCYANIDIN DIMERS AS THEIR PERACETATES AND OCTAMETHYL ETHER DIACETATES
Kolodziej, Herbert
, p. 1209 - 1216 (2007/10/02)
Key Word Index - Biomimetic synthesis; procyanidins B1-B8; 3,4-cis-biflavanoid; all--bi--(+)-catechin; 1H NMR parameters. Condensation of (2R,3S,4R or S)-leucocyanidin or the 5,7,3',4'-tetramethyl ether of (2R,3R,4S)-leucocyanidin with flavan-3-ols yielded dimeric flavanoids which were converted to their octamethyl ether diacetates, or the deca-acetates for the 2,3-trans-procyanidin series.Comparison is made of the 1H NMR spectra of the deca-acetate and octamethyl ether diacetate derivatives which lead to useful diagnostic shift parameters characteristic of their structures.Condensation afforded a novel biflavanoid with a 3,4-cis-configuration and a triflavanoid of 'mixed' stereochemistry.
Synthesis of Condensed Tannins. Part 13. The First 2,3-trans-3,4-cis-Procyanidins: Sequence of Units in a 'Trimer' of Mixed Stereochemistry
Delcour, Jan A.,Serneels, Edward J.,Ferreira, Daneel,Roux, David G.
, p. 669 - 676 (2007/10/02)
The condensation of (+)-leucocyanidin with (-)-epicatechin initiates a succession of substitutions leading mainly to the introduction of -2,3-trans-3,4-procyanidin units, but also to the incorporation of 'terminal' moieties which possess the hitherto unique 3,4-cis-procyanidin configuration.The bonding patterns in the products, and also the sequence of units in one of the 'trimers' of mixed stereochemistry, are resolved by (1)H n.m.r. spectroscopy through selective use of solvents at elevated temperatures.
Synthesis of Condensed Tannins. Part 9. The Condensation Sequence of Leucocyanidin with (+)-Catechin and with the Resultant Procyanidins
Delcour, Jan. A.,Ferreira, Daneel,Roux, David G.
, p. 1711 - 1717 (2007/10/02)
Molar equivalents of synthetic (2R,3S,4R of S)-leucocyanidin and (+)-catechin condense with exceptional rapidity at pH 5 under ambient conditions to give the all-trans-- and -bi- (procyanidins B3, B6) the all-trans-- and -tri- (procyanidin C2, and novel isomer), and the presumed all-trans--linked tetraflavanoid analogue in the proportions 10:1:12:1:3.The facility and sequence of these condensations correlate with the observed absence of leucocyanidins (flavan-3,3',4,4',5,7-hexaols) and also the dominance of related condensed tannins in plant extracts.
