9A Anthocyanins and Anthocyanin-Derived Compounds 443
structure/organoleptic properties (color and taste) relationship of the corresponding
reaction products is covered in Chapter 4.49D.
vinylflavanolsO
OHHOOH +
O
OROHR 1R 1R 1R 1 R^1R 1
R 1R 2R 2R 1
R 1
R 1R 2R 1R 3 R^4R 2R 1R 2R 5R 2R 1
R 2R 2R 2R 2 R 2R 2R 5R 2HOOHOHOH+
OOROH
HOOH+OOROH
HOOHOOH
HOOH
OHOH
CH 3 -CH CH 3 -CHO
OROH
HOOH
OOHOOHOHOHO+
OROH
HOOOH+
OOROH
HOOHOOR
HOOHOHOHO+OROH
HOO
COOH+OOROH
HOO+OOROH
HOOOHFlavanol-anthocyanin
adductsAnthocyanin-flavanol
adducts
flavanolsFlavanol-ethyl-
anthocyanin adductsFlavanyl-pyranoanthocyaninsacetaldehydeVitisinB-pyranoanthocyaninsVitisinA-
pyranoanthocyaninsvinylflavanols vinylphenolsFlavanyl-vinylpyranoanthocyanins
(Portisins)Hydroxyphenyl-
vinylpyranoanthocyaninsvinylphenolsor pyruvic acidHydroxyphenyl-
pyranoanthocyaninso-quinones of
caftaric acid (CA)CA-anthocyaninadductsOOHHOOHOHOH+
O
OROH
HOOO+
OROH
HOO
OHHOOHOHOHO(c) (b) (d) (e)+OOROH
HOOHOHOHHCOC
COOHCOOHOHC OH(a)(f)(j) (k)(i)(g)(h)flavanols,
acetaldehydeAnthocyanin-ethyl-
anthocyanin dimersFig. 9A.3Main chemical reactions of anthocyanins during winemaking
9A.2.1 Reactions of Anthocyanins with Enzymatically Generated
o-Quinones
Precursors.Precursors for this reaction are anthocyanins ando-quinones of caf-
feoyltartaric (caftaric acid) andp-coumaroyltartaric (cutaric acid) acids generated
by enzymatic oxidation by grape polyphenoloxidase (PPO) (Singleton et al. 1985).
PPO first adds an OH group to monophenols and then oxidizes the resultingo-
diphenol too-quinone.
Mechanism of reaction.Under oxidative conditions and for grapes containing
high levels of hydroxycinnamic acids and low of levels of glutathione (a com-
pound that easily reacts witho-quinones, preventing oxidation of phenolic com-
pounds in wines) (Sarni-Manchado et al. 1995), some phenolics are able to react
with theo-quinones of caftaric acid (Cheynier et al. 1986) (see also Chapter 9B).