Abstract
Many have spoken and written concerning the motivations which inspire a scientist in his work. For some there is an inherent curiosity about the workings of nature, and for others, the inspiration comes from the desire to make significant and lasting contributions to human knowledge. It would nevertheless be idle to deny that for a scientist the recognition of his work by his peers is an event which engenders the deepest personal satisfaction. I should therefore like to express to all those who have been responsible for this award and the decision to bestow it upon me, my sincere thanks. Much, much more importantly by honoring me you also honor my many colleagues who, over the years, have participated in this endeavor. It gives me enormous pleasure to record my gratitude to them.
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References
Bate-Smith, E.C.; Swain, T. In: Mason, H.S.; Florkin, A.M. (eds.). Comparative biochemistry, vol. 3. Academic Press, New York, p. 764 (1962).
Haslam, E. Plant polyphenols—vegetable tannins re-visited. Cambridge University Press, Cambridge, 230 pp. (1989).
Haslam, E. Practical polyphenolics: from structure to molecular recognition and physiological action. Cambridge University Press, Cambridge, 420 pp. (1998).
Porter, L.J. Flavans and proanthocyanidins. In: Harborne, J.B. (ed.). The flavanoids: Advances in research since 1980. Chapman and Hall, London, p. 21, (1988).
Porter, L.J. Tannins. In: Harborne, J.B. (ed.). Methods in plant biochemistry. Academic Press, London and New York, p. 389 (1989).
Bate-Smith E.C.; Metcalfe C.R. Leucoanthocyanins. 3._The nature and systematic distribution of tannins in dicotyledenous plants. Biochem. J. 55:669 (1957).
Mole, S. The systematic distribution of tannins in the leaves of angiosperms: a tool for ecological studies. Biochemical Systematics and Ecology, 21:833 (1993).
Robinson R.; Robinson G.M. A survey of anthocyanins. III. Notes on the distribution of leuco-anthocyanins. Biochem. J. 27:206 (1933).
Okuda T.; Hatano T.; Yoshida T. New methods of analysing tannins. J. Nat. Prod. 52:1 (1989).
Okuda, T.; Hatano, T.; Yoshida, T. Oligomeric hydrolysable tannins, a new class of plant polyphenol. Heterocycles, 30:1195 (1990).
Haslam, E.; Cai, Y. Plant polyphenols (vegetable tannins): gallic acid metabolism. Natural Products Reports (Roy. Soc. Chem.) 11:44 (1994).
Schmidt O.Th.; Mayer W. Naturliche gerbstoffe. Angew. Chem. 68:103 (1956).
Glombitza, K.; Gerstberger; G. Phlorotannins with dibenzodioxin structural elements from the brown alga Eisenia arborea. Phytochemistry 24:543 (1985).
Ragan M.A. The high molecular weight polyphloroglucinols of the marine brown alga Fucus vesiculosus. Can. J. Chem. 63:294 (1985).
McInnes A.G.; Smith D.G.; Walter J.A.; Ragan M.A. The high molecular weight polyphloroglucinols of the marine brown alga Fucus vesiculosus: 1H and 13C nuclear magnetic resonance spectroscopy. Can. J. Chem. 63:304 (1985).
Hillis W.E.; Swain T. The phenolic constituents of Prunus domestica. II. The analysis of tissues of the Victoria plum tree. J. Sci. Food Agric. 10:135 (1959).
Bate-Smith E.C. Tannins of the herbaceous Leguminosae. Phytochemistry 12:1809 (1973).
Shen Z.; Haslam E.; Falshaw C.P.; Begley M.J. Procyanidins and polyphenols of Larix gmelini bark. Phytochemistry 25:2629 (1986).
Somers T.S. The polymeric nature of wine pigments. Phytochemistry 10:2175 (1971).
Roberts, E.A.H. Economic importance of flavonoid substances: tea fermentation. In: Geissman, T.A. (ed.). The chemistry of flavanoid compounds, Pergamon Press, Oxford, London and New York, p. 468 (1962).
Mayer, W.; Hoffmann, E.H.; Losch, N.; Wolf, H.; Wolter, B.; Schilling, G. Dehydrierungsreaktionem mit gallusaureestern. Liebig’s Annalen de Chemie:929-938 (1984).
Waterhouse, A.L. Wine and heart disease. Chem. Ind. p. 338 (1995).
Haslam E. Natural polyphenols (vegetable tannins) as drugs: possible modes of action. J. Nat. Prod. 59:205 (1996).
Haslam E. The metabolism of gallic and hexahydroxydiphenic acid in plants. Fortschritt. Chem. Org. Naturstoffe 41:1 (1982).
Haslam E. Hydroxybenzoic acids and the enigma of gallic acid. In: Conn, E.E. (ed.). The shikimic acid pathway. Recent Advances in Phytochemistry 20:163 (1986).
Zenk, M.H. Zur frage de biosynthese von gallusaure. Z. Naturforsch. 19B:83 (1964).
Knowles, P.F.; Haslam, E.; Haworth, R.D. Gallotannins. Part 4._The biosynthesis of gallic acid. J. Chem. Soc.:1854 (1961).
Cornthwaite, D.C.; Haslam, E. Gallotannins. Part 9._The biosynthesis of gallic acid in Rhus typhina. J. Chem. Soc.:3008 (1965).
Dewick P.M.; Haslam E. Phenol biosynthesis in higher plants—gallic acid. Biochem. J. 113:537 (1969).
Gross G.G.; Denzel K.; Schilling G. Biosynthesis of gallotannins. Enzymatic conversion of 1,6-digalloylglucose to 1,2,6-trigalloylglucose. Planta 176:135 (1988).
Gross, G.G.; Denzel, K. Biosynthesis of gallotannins. β-Glucogallin dependent galloylation of 1,6-digalloylglucose to 1,2,6-trigalloylglucose. Z. Naturforsch. 46C:389 (1991).
Richardson A.C.; Williams J.M. Selective acylation of pyranosides. I. Benzoylation of α-methylpyranosides of mannose, glucose and galactose. Tetrahedron 23:1369 (1967).
Haslam, E. Secondary metabolism—evolution and function; products or processes? Chemoecology 5/6:89 (1994/1995).
Hahlbrock K.; Scheel D. Physiology and molecular biology of phenylpropanoid metabolism. Ann. Rev. Plant Physiol. 40:347 (1989).
Stafford H.A.; Lester H.H. Flavan-3-ol biosynthesis. The conversion of (+)-dihydroquercetin and flavan-3,4-diol (leucocyanidin) to (+)-catechin by reductases extracted from cell suspension cultures of Douglas fir. Plant Physiol. 76:184 (1984).
Stafford H.A.; Lester H.H. Flavan-3-ol biosynthesis. The conversion of (+)-dihydromyricetin to its flavan-3,4-diol (leucodelphinidin) and (+)-gallocatechin by reductases extracted from cell suspension cultures of Gingko biloba and Pseudostuga menziesii. Plant Physiol. 76:184 (1985).
Stafford H.A.; Lester H.H.; Porter L.J. Chemical and enzymic synthesis of monomeric procyanidins (leucocyanidins) from 2R, 3R-dihydroquercetin. Phytochemistry 24:333 (1985).
Haslam, E. Biogenetically patterned synthesis of procyanidins. J. Chem. Soc. Chemical Commun.:594 (1974).
Hemingway, R.W.; Foo, L.Y. Quinone methide intermediates in procyanidin synthesis. J. Chem. Soc. Chemical Commun.:1035 (1983).
Haslam E. Symmetry and promiscuity in proanthocyanidin biochemistry. Phytochemistry 16:1625 (1977).
Fraenkel G. The raison d’etre of secondary plant substances. Science 129:1466 (1959).
Feeny P. Plant apparency in chemical defence. Rec. Adv. Phytochemistry 10:1 (1976).
Rhoades D.F.; Cates R.G. Toward a general theory of plant herbivore chemistry. Rec. Adv. Phytochemistry 10:168 (1976).
Muller C.H. Co-evolution. Science 165:415 (1969).
Cairns-Smith, A.G. Seven clues to the origin of life. Cambridge University Press, Cambridge (1985).
Feeny P. Effects of oak leaf tannins on larval growth of the winter moth Operophthera brumata. J. Insect Physiol. 14:805 (1968).
Feeny P. Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51:565 (1970).
Bate-Smith E.G. Haemanalysis of tannins—the concept of relative astringency. Phytochemistry 12:907 (1973).
Beart J.E.; Haslam E.; Lilley T.E. Plant polyphenols—secondary metabolism and chemical defence. Phytochemistry 24:33 (1985).
Atkinson, D.E. Cellular energy metabolism and its regulation. Academic Press, New York (1977).
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Haslam, E. (1999). Che Farò Senza Polifenoli?. In: Gross, G.G., Hemingway, R.W., Yoshida, T., Branham, S.J. (eds) Plant Polyphenols 2. Basic Life Sciences, vol 66. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-4139-4_2
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