Phytochemicals in Human Health Protection, Nutrition, and Plant Defense 1999
DOI: 10.1007/978-1-4615-4689-4_10
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Recent Advances in the Chemistry of Proanthocyanidins

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Cited by 4 publications
(6 citation statements)
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“…From a chemical point of view, PACs are oligomers or polymers resulting from the condensation of two or more 2-phenyl-3,4-dihydro-2H-chromen-3-ol (flavan-3-ol) units, which are composed of two aromatic benzyl rings joined by three carbon atoms that form an oxygenated heterocyclic ring (C6-C3-C6) ( Figure 1 A). In this context, oligomers derive from the condensation of 2–5 flavan-3-ol units, meanwhile polymers are much larger and derived by the condensation of 6–60 units [ 11 , 12 , 13 ]. Unlike other flavonoids, flavan-3-ols and, consequently PACs, have saturated A-ring and, hence, are non-planar molecules [ 14 ].…”
Section: Chemistrymentioning
confidence: 99%
See 1 more Smart Citation
“…From a chemical point of view, PACs are oligomers or polymers resulting from the condensation of two or more 2-phenyl-3,4-dihydro-2H-chromen-3-ol (flavan-3-ol) units, which are composed of two aromatic benzyl rings joined by three carbon atoms that form an oxygenated heterocyclic ring (C6-C3-C6) ( Figure 1 A). In this context, oligomers derive from the condensation of 2–5 flavan-3-ol units, meanwhile polymers are much larger and derived by the condensation of 6–60 units [ 11 , 12 , 13 ]. Unlike other flavonoids, flavan-3-ols and, consequently PACs, have saturated A-ring and, hence, are non-planar molecules [ 14 ].…”
Section: Chemistrymentioning
confidence: 99%
“…The most famous example of this condition is represented by the catechin, which has been detected and identified in all four different forms ( Figure 1 C). In order to form a PAC, each flavan-3-ol unit is linked to another unit through C–C and/or C–O bonds [ 12 , 17 , 19 ]. The most usual linkages are C–C bonds established between the C 4 of one flavan-3-ol unit and C 8 or C 6 of another ( Figure 2 A).…”
Section: Chemistrymentioning
confidence: 99%
“…Remarkably, no tannins, except for proteracacinidin-type oligomers, exist in this species [ 93 ]. Their synthesis might result from the monomeric flavan-3,4-diol precursors’ pyrogallol A-ring losing its nucleophilicity, allowing alternate centers to take part in the formation of the interflavanyl bonding process [ 104 ]. These agents are complemented by flavonol, dihydroflavonol, flavanone, proteracacinidin dimers, and chalcone analogs [ 105 ].…”
Section: Chemical Components Isolated From Acaciamentioning
confidence: 99%
“…Due to its nutraceutical properties, buttermilk is considered a beneficial ingredient for infant formulas, as it is related to many health benefits such as prevention of colon cancer (Dewettinck et al, 2008;Fuller et al, 2013;Spitsberg, 2005;Sprong et al, 2002;Ward et al, 2009). Buttermilk used as raw material in the food industry undergoes processes such as homogenization, pasteurization, dehydration by evaporation and/or spray drying (Ferreira et al, 1999;Vanderghem et al, 2010). Buttermilk powder can be used as a partial substitute for solids in various products as baked goods and yogurt (Hickey et al, 2018;Scalbert et al, 2005).…”
Section: Introductionmentioning
confidence: 99%