The Direct Biomimetic Synthesis, Structure and Absolute Configuration of Angular and Linear Condensed Tannins

Author:

Roux D. G.,Ferreira D.

Publisher

Springer Vienna

Reference27 articles.

1. Creasy, L. L., and T. Swain: Structure of condensed tannins. Nature 208, 151 (1965).

2. Geissman, T. A., and N. N. Yoshimura: Synthetic proanthocyanidin. Tetrahedron Letters 1966, 2669.

3. Pelter, A., and P. I. Amenechi: Isoflavonoid and pterocarpinoid extractives of Lonchocarpus laxiflorus. J. Chem. Soc. (C) 1969, 887; Pelter, A., P. I. Amenechi, R. Warren and S. H. Harper: The structures of two proanthocyanidins from Julbernadia globiflora. J. Chem. Soc. (C) 1969, 2572.

4. Engel, D. W., M. Hattingh, H. K. L. Hundt, and D. G. Roux: X-ray structure, conformation, and absolute configuration of 8-bromotetra-0-methyl-(+)-catechin. J. Chem. Soc. Chem. Commun. 1978, 695.

5. Hundt, H. K. L., and D. G. Roux: Condensed tannins: Determination of the point of linkage in “terminal” (+)-catechin units and degradative bromination of 4-flavanylflavan-3,4-diols. J. Chem. Soc. Chem. Commun. 1978, 696.

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