The structure of the proanthocyanidin B-2 dimer was proved to be (-)ep
icatechin-(4 beta-8)-(-)epicatechin by two-dimensional heteronuclear N
MR spectroscopy. The compound adopts two conformations in solution, in
which the interflavan dihedral angles are roughly +/- 90 degrees. The
preferred conformation of the pyran ring is a half-chair with the 3',
4'-dihydroxyphenyl substituents in pseudo-equatorial positions. (C) 19
97 John Wiley & Sons, Ltd.