Issue 16, 1997

Rational design, synthesis and biological evaluation of the first inhibitor of lignin polymerization

Abstract

A fluorinated analogue of coniferin (the glucoside of coniferyl alcohol) has been synthesized in three steps from vanillin tetraacetyl glucoside; bearing a fluorine atom on the β position of the propenyl side chain which is involved in the main site of coupling, it is designed as a potential inhibitor of oxidases involved in the biosynthesis of lignin, and in vivo experiments show a pronounced inhibition of lignin biosynthesis in poplar plantlets, with a five-fold decrease in lignin formed.

Article information

Article type
Paper

Chem. Commun., 1997, 1489-1490

Rational design, synthesis and biological evaluation of the first inhibitor of lignin polymerization

N. Daubresse, Y. Chupeau, C. Francesch, C. Lapierre, B. Pollet and C. Rolando, Chem. Commun., 1997, 1489 DOI: 10.1039/A702464I

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