Results 91 to 100 of about 12,719 (269)

Synthesis of 4-Pyridone-3-sulfate and an improved synthesis of 3-Hydroxy-4-Pyridone [PDF]

open access: yesChemistry Central Journal, 2009
An improved synthesis of 3-hydroxy-4-pyridone via an Elbs oxidation of 4-pyridone and isolation of 4-pyridone-3-sulfate is described.
openaire   +4 more sources

Designing Enzymatic Reactivity with an Expanded Palette

open access: yesChemBioChem, Volume 26, Issue 11, June 3, 2025.
Innovation in biocatalysis is rapidly increasingly the diversity of catalytic reactivity that can be mediated by enzymes, addressing a key bottleneck for their widespread adoption in industrial chemical synthesis. A key approach to this is building enzymes with unnatural catalytic components that provide an expanded palette with new possibilities for ...
Reuben B. Leveson‐Gower
wiley   +1 more source

Synthesis of New Potentially Bioactive Bicyclic 2-Pyridones

open access: yesMolecules, 2005
Three convenient methods of reduction of the nitro group of 5-nitroimidazoles and 5-nitrothiazole that bear a diethylmethylene malonate group in an ortho-like position with respect to the nitro group and cyclization of the resulting amino derivatives are
Patrice Vanelle   +3 more
doaj   +1 more source

Organometallic catalysis for applications in radical chemistry and asymmetric synthesis [PDF]

open access: yes, 2014
Two organometallic catalysis studies are presented. The first one deals with the development of a new catalytic agent based on the mixture of a hydride and an iron salt to trigger efficient radical cyclization processes.
Ateywiohrera   +17 more
core   +2 more sources

Noninvasive Evaluation of Prolonged‐Release Pirfenidone in Compensated Liver Cirrhosis. ODISEA Study, a Randomised Trial

open access: yesLiver International, Volume 45, Issue 6, June 2025.
ABSTRACT Background Advanced liver fibrosis (ALF) predicts an adverse prognosis in chronic liver disease. In addition to etiological treatment, a new approach to stop or reverse residual fibrosis is desirable. Objective To assess the efficacy and safety of prolonged‐release pirfenidone (PR‐PFD) versus placebo in compensated cirrhosis.
Linda E. Muñoz‐Espinosa   +17 more
wiley   +1 more source

Synthesis of a Pyridone ALkaloid, Cerpegin.

open access: yesChemical and Pharmaceutical Bulletin, 1995
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Takahiko Arase, Keizo Matsuo
openaire   +4 more sources

Phenacylation of 6-Methyl-Beta-Nitropyridin-2-Ones and Further Heterocyclization of Products

open access: yesMolecules, 2020
Reaction between the derivatives of 6-methyl-beta-nitropyridin-2-one and phenacyl bromides was studied, and the yields observed were extremely low. The pyridones were converted via chloropyridines to methoxyderivatives, which were N-phenacylated.
Eugene V. Babaev, Victor B. Rybakov
doaj   +1 more source

Study on the Lewis Acid-promoted Aza-Diels - Alder Reaction of Azetidin-2-one-tethered Imines with Siloxydienes in the Asymmetric Synthesis of 2-Aryl(alkyl)-2,3-dihydro-4-pyridones [PDF]

open access: yes, 2008
trans-3-Amino-b-lactams were evaluated as the chiral building blocks in the aza-Diels – Alder reaction of azetidin-2-one-tethered imines with siloxydienes under Lewis acid catalysis, as a route for the asymmetric synthesis of 2-aryl(alkyl)-2,3-dihydro ...
Habuš, Ivan   +3 more
core   +1 more source

Activation of Small Molecules by Readily Accessible Alkylborane‐Based Frustrated Lewis Pairs

open access: yesEuropean Journal of Inorganic Chemistry, Volume 28, Issue 15, May 28, 2025.
Simple alkylborane‐based frustrated Lewis pairs (FLPs) are demonstrated to activate hydrogen, ammonia, the NH bond of secondary amines, and the CH bonds of terminal alkynes, highlighting the potential of readily accessible FLPs for small‐molecule activation.
Arthur Averdunk   +3 more
wiley   +1 more source

One-pot Synthesis of 6-Aza-chromone Derivatives Through Cascade Carbonylation-Sonogashira-Cyclization

open access: yesScientific Reports, 2017
We developed an efficient synthesis of aza-chromones from 3-iodo-4-(1H)-pyridones and terminal acetylenes via a cascade carbonylation-Sonogashira-cyclization reaction.
Gang Cheng   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy