Articles with "fecl3 catalyzed" as a keyword



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FeCl3-catalyzed ethanol pretreatment of sugarcane bagasse boosts sugar yields with low enzyme loadings and short hydrolysis time.

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Published in 2018 at "Bioresource technology"

DOI: 10.1016/j.biortech.2017.10.053

Abstract: An organosolv pretreatment system consisting of 60% ethanol and 0.025 mol·L-1 FeCl3 under various temperatures was developed in this study. During the pretreatment, the highest xylose yield was 11.4 g/100 g raw material, representing 49.8% of xylose in… read more here.

Keywords: fecl3 catalyzed; hydrolysis time; sugarcane bagasse; hydrolysis ... See more keywords
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A direct FeCl3-catalyzed cross-coupling and cyclization reactions: A new approach to the construction of functionalized pyrano[3,2-a]carbazole derivatives

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Published in 2017 at "Tetrahedron"

DOI: 10.1016/j.tet.2017.06.059

Abstract: Abstract The FeCl3-catalyzed cross-coupling through a sequential C−N and C−C bond-forming via tandem C−H and N−H bonds functionalization represents a novel method for the formation of dimeric carbazole derivatives. This approach provides a novel dimeric… read more here.

Keywords: fecl3 catalyzed; pyrano carbazole; carbazole derivatives; catalyzed cross ... See more keywords
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FeCl3-catalyzed three-component aryl-selenylation of alkenes

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Published in 2021 at "Tetrahedron"

DOI: 10.1016/j.tet.2021.132239

Abstract: Abstract FeCl3-catalyzed three-component aryl-selenylation of alkenes with good to excellent yields has been disclosed. This method is characterized by synthesis of complicated products in a single-step reaction, simple operation and readily available commercially reagents. Finally,… read more here.

Keywords: fecl3 catalyzed; aryl selenylation; three component; catalyzed three ... See more keywords
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FeCl3-catalyzed sequential cyclization for the construction of 12-aryl 5,7-dihydropyrido[2,3-b:6,5-b']diindoles

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Published in 2020 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2020.152334

Abstract: Abstract A facile approach to prepare 12-aryl 5,7-dihydropyrido[2,3-b:6,5-b']diindoles via tandem cyclizations is described. FeCl3 is used as the catalyst for the reaction between o-aminophenylacetonitriles and aromatic aldehydes, generating 5,7-dihydropyrido[2,3-b:6,5-b']diindoles derivatives in moderate to high yields. read more here.

Keywords: fecl3 catalyzed; dihydropyrido diindoles; dihydropyrido; sequential cyclization ... See more keywords
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I2/FeCl3-Catalyzed Domino Reaction of Aurones with Enamino Esters for the Synthesis of Highly Functionalized Pyrroles.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c03537

Abstract: A novel and efficient I2/FeCl3-catalyzed domino reaction of aurones with enamino esters via Michael addition, iodination, intramolecular nucleophilic substitution, and spiro ring opening processes has been developed, affording a vast variety of polysubstituted pyrroles in… read more here.

Keywords: reaction; fecl3 catalyzed; domino reaction; aurones enamino ... See more keywords
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Facile Extraction of Thermally Stable and Dispersible Cellulose Nanocrystals with High Yield via a Green and Recyclable FeCl3-Catalyzed Deep Eutectic Solvent System

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Published in 2019 at "ACS Sustainable Chemistry & Engineering"

DOI: 10.1021/acssuschemeng.9b00209

Abstract: In the current work, a green and recyclable FeCl3-catalyzed deep eutectic solvent system (F-DES) was invented to fabricate cellulose nanocrystals (CNCs) with a high yield and excellent thermal stability. It was found that the optimum… read more here.

Keywords: high yield; fecl3 catalyzed; deep eutectic; eutectic solvent ... See more keywords