Results 11 to 20 of about 49,888 (203)

One-step synthesis of pyridines and dihydropyridines in a continuous flow microwave reactor [PDF]

open access: yes, 2013
The Bohlmann–Rahtz pyridine synthesis and the Hantzsch dihydropyridine synthesis can be carried out in a microwave flow reactor or using a conductive heating flow platform for the continuous processing of material. In the Bohlmann–Rahtz reaction, the use
Bagley, Mark C   +4 more
core   +2 more sources

Fast microwave-assisted oxidation of 1,4-dihydropyridines with FeCl 3.SiO 2 [PDF]

open access: yes, 2005
Pyridine derivatives are easily obtained in high yields by microwave-promoted rapid oxidation of the corresponding 1,4-dihydropyridines with ferric chloride hexahydrate and silica gel under solvent-free ...
Alaee, E.   +4 more
core   +1 more source

Synthesis of Chitosan-La2O3 Nanocomposite and Its Utility as a Powerful Catalyst in the Synthesis of Pyridines and Pyrazoles

open access: yesMolecules, 2021
Recently, the development of nanocatalysts based on naturally occurring polysaccharides has received a lot of attention. Chitosan (CS), as a biodegradable and biocompatible polysaccharide, is considered to be an excellent template for the design of a ...
Khaled D. Khalil   +4 more
doaj   +1 more source

Degradation of lansoprazole and omeprazole in the aquatic environment [PDF]

open access: yes, 2006
Lansoprazole and omeprazole degrade in water leading to sulfides, benzimidazolones and a red complex material. Degradation is accelerated in acid medium and by solar simulator irradiation.
BRIGANTE M.   +5 more
core   +1 more source

4-(Methylamino)pyridine [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
The non-H atoms of the title compound, C(6)H(8)N(2), lie in a common plane (r.m.s. deviation = 0.034 Å). In the crystal, adjacent mol-ecules are linked by inter-molecular N-H⋯N hydrogen bonds into a zigzag chain running along the c axis.
openaire   +3 more sources

Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates [PDF]

open access: yes, 2014
This tutorial review highlights the organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium/azolium enolates.
Morrill, Louis C., Smith, Andrew D.
core   +1 more source

Quaterpyridine Ligands for Panchromatic Ru(II) Dye Sensitizers [PDF]

open access: yes, 2012
A new general synthetic access to carboxylated quaterpyridines (qpy), of interest as ligands for panchromatic dyesensitized solar cell organometallic sensitizers, is presented.
Abbotto, Alessandro   +6 more
core   +1 more source

Highly enantioselective catalytic synthesis of chiral pyridines

open access: yesNature Communications, 2017
Chiral pyridines are valuable building blocks in medicinal chemistry applications. Here, the authors report the copper-catalysed Lewis acid-assisted asymmetric alkylation of β-substituted alkenyl pyridines with Grignard reagents affording chiral ...
Ravindra P. Jumde   +3 more
doaj   +1 more source

Synthesis, Molecular Docking Study, and Cytotoxicity Evaluation of Some Novel 1,3,4-Thiadiazole as Well as 1,3-Thiazole Derivatives Bearing a Pyridine Moiety

open access: yesMolecules, 2022
Pyridine, 1,3,4-thiadiazole, and 1,3-thiazole derivatives have various biological activities, such as antimicrobial, analgesic, anticonvulsant, and antitubercular, as well as other anticipated biological properties, including anticancer activity.
Amr S. Abouzied   +7 more
doaj   +1 more source

[2,2′-Bipyridin]-6(1H)-one, a Truly Cooperating Ligand in the Palladium-Mediated C–H Activation Step: Experimental Evidence in the Direct C-3 Arylation of Pyridine [PDF]

open access: yes, 2018
Producción CientíficaThe ligand [2,2′-bipyridin]-6(1H)-one (bipy-6-OH) has a strong accelerating effect on the Pd- catalyzed direct arylation of pyridine or arenes.
Albéniz Jiménez, Ana Carmen   +2 more
core   +4 more sources

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