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1.
Bioresour Technol ; 373: 128752, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-36804856

RESUMEN

The fermented corn stover residues are abundant renewable lignin-rich bioresources that show great potential to produce aromatic phenols. However, selective catalytic hydrogenolysis of this residual material still remains challenge to obtain high yields. Herein, a novel strategy to produce monophenolic compounds from the fermented stover over a commercial Pd/C catalyst was proposed. Taking the reaction temperature as the key variable, the highest monomer yield was 28.5 wt% at 220 °C in compaction with that of the pristine corn stover (22.8 wt%). The enhanced monophenol yield was due to the higher contents of lignin and less recalcitrance in the fermented stover. Moreover, the van Krevelen diagram revealed a slight selective CO bond scission of lignin macromolecular during fermentation as well as the dehydration and deoxygenation in hydrogenolysis reaction. Overall, this work opens a new avenue for the valorization of lignin through reductive catalytic fractionation of agricultural wastes.


Asunto(s)
Lignina , Zea mays , Lignina/química , Zea mays/química , Catálisis , Fraccionamiento Químico , Fenoles
2.
Mol Divers ; 20(3): 611-8, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26880591

RESUMEN

The synthesis of novel coumarin[8,7-e][1,3]oxazine derivatives through a microwave-assisted three-component one-pot Mannich reaction is described in this study. All the target compounds were evaluated in vitro for their antifungal activity against Botrytis cinerea, Colletotrichum capsici, Alternaria solani, Gibberella zeae, Rhizoctonia solani, and Alternaria mali. The preliminary bioassays showed that 5e, 5m, and 5s exhibited good antifungal activity and the most active compound was 5m with an [Formula: see text] value as low as 2.1 nM against Botrytis cinerea.


Asunto(s)
Antifúngicos/síntesis química , Cumarinas/química , Oxazinas/síntesis química , Antifúngicos/química , Antifúngicos/farmacología , Técnicas Químicas Combinatorias , Hongos/efectos de los fármacos , Microondas , Estructura Molecular , Oxazinas/química , Oxazinas/farmacología , Relación Estructura-Actividad
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