EFFECTS OF HCN, PHENOLIC ACIDS AND RELATED COMPOUNDS IN SORGHUM BICOLOR ON THE FEEDING BEHAVIOUR OF THE PLANTHOPPER PEREGRINUS MAIDIS

1980 ◽  
Vol 27 (3) ◽  
pp. 211-222 ◽  
Author(s):  
J. FISK
2015 ◽  
Vol 48 (2) ◽  
pp. 317-325 ◽  
Author(s):  
Koho Saito

Quantitative variation of nine flavonoid compounds and two related phenolic acids in several parts of three garden varieties of <i>Cosmos bipinnatus</i> Cav. were examined by; means of paper chromatography followed by a spectrophotometric procedure.


2021 ◽  
Vol 11 (18) ◽  
pp. 8276
Author(s):  
Oscar Vidal-Casanella ◽  
Oscar Núñez ◽  
Mercè Granados ◽  
Javier Saurina ◽  
Sonia Sentellas

Phenolic compounds such as phenolic acids, flavonoids, and stilbenes comprise an enormous family of bioactive molecules with a range of positive properties, including antioxidant, antimicrobial, or anti-inflammatory effects. As a result, plant extracts are often purified to recover phenolic compound-enriched fractions to be used to develop nutraceutical products or dietary supplements. In this article, we review the properties of some remarkable plant-based nutraceuticals in which the active molecules are mainly polyphenols and related compounds. Methods for the characterization of these extracts, the chemical determination of the bioactivities of key molecules, and the principal applications of the resulting products are discussed in detail.


2010 ◽  
Vol 58 (16) ◽  
pp. 9214-9220 ◽  
Author(s):  
Louise Svensson ◽  
Bonno Sekwati-Monang ◽  
Daise Lopes Lutz ◽  
Andreas Schieber ◽  
Michael G. Gänzle

1984 ◽  
Vol 14 (1) ◽  
pp. 45-51 ◽  
Author(s):  
Stanley Z. Dziedzic ◽  
Bertram J.F. Hudson

1979 ◽  
Vol 7 (4) ◽  
pp. 309-310 ◽  
Author(s):  
Susan Woodhead ◽  
Gillian Cooper-Driver

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 37 ◽  
Author(s):  
Immacolata C. Tommasi

This review focuses on recent advances in the field of enzymatic carboxylation reactions of hydroxyaromatic compounds using HCO3− (as a CO2 source) to produce hydroxybenzoic and other phenolic acids in mild conditions with high selectivity and moderate to excellent yield. Nature offers an extensive portfolio of enzymes catalysing reversible decarboxylation of hydroxyaromatic acids, whose equilibrium can be pushed towards the side of the carboxylated products. Extensive structural and mutagenesis studies have allowed recent advances in the understanding of the reaction mechanism of decarboxylase enzymes, ultimately enabling an improved yield and expansion of the scope of the reaction. The topic is of particular relevance today as the scope of the carboxylation reactions can be extended to include lignin-related compounds in view of developing lignin biorefinery technology.


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