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1
Published in 2019 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/s10593-019-02584-5
Abstract: Alkylation of 6-methyl-4-thioxo-4,5-dihydrofuro[3,4-c]pyridin-3(1H)-one in an alkaline medium proceeds regioselectively at the sulfur atom to form sulfanyl derivatives.
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Keywords:
methyl sulfanylfuro;
methyl;
synthesis novel;
sulfanylfuro pyridin ... See more keywords
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0
Published in 2020 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/s10593-020-02832-z
Abstract: The three-component condensation of pyridinium acylmethylides generated in situ with aromatic aldehydes and 4-hydroxy-6-methylpyridones gave a series of 2-acyl-3-aryl-3,5-dihydrofuro[3,2-c]pyridin-4(2H)-ones. The reaction proceeds diastereoselectively with the formation of trans-isomers and represents a cascade process involving the…
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Keywords:
dihydrofuro pyridin;
regio diastereoselective;
pyridin ones;
acyl aryl ... See more keywords
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Published in 2018 at "Bioorganic chemistry"
DOI: 10.1016/j.bioorg.2018.09.013
Abstract: New azafluorenones, 2-aryl-4-(4-hydroxyphenyl)-5H-indeno[1,2-b]pyridin-5-ones, were prepared to evaluate their cytotoxic/anticancer properties, also their inhibitory effects on hCA I and II isoenzymes. Aryl part was changed as [phenyl (H1), 4-methylphenyl (H2), 4-methoxyphenyl (H3), 4-fluorophenyl (H4), 4-bromophenyl (H5),…
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Keywords:
new azafluorenones;
hydroxyphenyl indeno;
pyridin ones;
aryl hydroxyphenyl ... See more keywords
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Published in 2017 at "European journal of medicinal chemistry"
DOI: 10.1016/j.ejmech.2016.09.075
Abstract: A series of 3,7-diaryl-6,7-dihydroisothiazolo [4,5-b]pyridin-5(4H)-ones 8 and 9 was synthesized by multicomponent condensation of 3-aryl-5-isothiazolecarboxylic acid esters 4a-f with aromatic (or thienyl) aldehydes 7 and Meldrum's acid in an acidic medium. The targeted compounds were…
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Keywords:
pyridin ones;
cell based;
synthesis anti;
cell ... See more keywords
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2
Published in 2023 at "Journal of medicinal chemistry"
DOI: 10.1021/acs.jmedchem.2c02044
Abstract: Pseudomonas aeruginosa infections are often complicated by the fact that it can easily form a biofilm that increases its resistance to antibiotics. Consequently, the development of novel antibacterial agents against biofilm-associated drug-resistant P. aeruginosa is…
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Keywords:
pseudomonas aeruginosa;
ciprofloxacin conjugates;
pyridin ones;
hydroxy pyridin ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c01513
Abstract: We developed a novel asymmetric Friedel-Crafts alkylation/transamidation tandem reaction for the enantio- and diastereoselective synthesis of pyrazolo[3,4-b]pyridin-6-ones bearing a -CF3 unit via synergistic chiral phosphoric acid and MgSO4 catalysis. This [3 + 3] annulation protocol…
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Keywords:
trifluoromethylated pyrazolo;
chiral phosphoric;
acid mgso4;
pyridin ones ... See more keywords
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0
Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.8b02003
Abstract: Fluorination of 2-aminopyridines and pyridin-2(1 H)-ones in the presence of Selectfluor, water, and chloroform under mild conditions has been realized. This method gives fluorinated pyridines in good to high yields with high regioselectivities. The electron-deficient…
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Keywords:
selective fluorination;
aminopyridines pyridin;
pyridin ones;
fluorination ... See more keywords
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Published in 2018 at "Synlett"
DOI: 10.1055/s-0037-1610171
Abstract: A conceptually new synthesis of pyridine rings by a [C4 + CN] assembly has been developed by applying a vinylogous version of the classic Blaise reaction. The zinc-mediated reaction of (het)aryl or alkyl nitriles with…
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Keywords:
new synthesis;
blaise reaction;
pyridin ones;
reaction ... See more keywords