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8-methylquinoline

National Institutes of Health

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Quinolines

Papers overview

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2019
2019
Rh(iii)-Catalyzed straightforward arylation of 8-methyl/formylquinolines using diazo compounds.
A straightforward Rh(iii)-catalyzed general strategy was developed for the introduction of naphthol/phenol moieties to the C(sp3… 
2014
2014
The MCH1 receptor, an anti‐obesity target, is allosterically inhibited by 8‐methylquinoline derivatives possessing subnanomolar binding and long residence times
Melanin‐concentrating hormone receptor 1 (MCH1 receptor) antagonists are being considered as anti‐obesity agents. The present… 
Highly Cited
2013
Highly Cited
2013
Optimizing P,N-bidentate ligands for oxidative gold catalysis: efficient intermolecular trapping of α-oxo gold carbenes by carboxylic acids.
Steric Bulk or Conformation Control? Optimization of P,N-bidentate ligands reveals the importance of conformation control in the… 
2004
2004
Inclusion of quinolines by binaphthol: structures and selectivity.
The enclathration selectivity of the host compound 2,2'-dihydroxyl-1,1'-binaphthyl, BINAP, towards the guests quinoline (Q), 2… 
2000
2000
A donor-acceptor compound composed of a dinuclear zinc(II) complex of a robson macrocycle with 8-methylquinoline
A donor-acceptor compound, diaqua-1kappaO,2kappaO-[&mgr;-11, 23-dimethyl-3,7,15,19-tetraazatricyclo[19.3.1.1(9,13)]hexacosa-1(25… 
1991
1991
Genotoxicity of fluoroquinolines and methylquinolines.
Quinoline in the presence of microsomal activation exhibits mutagenic activity in Salmonella typhimurium TA100 and induces… 
1980
1980
Carbon-hydrogen bond activation in transition metal compounds
Abstract 
1973
1973
Nitramine — A new alkaloid from Nitraria schoberi
SummaryA new liquid base with the composition C10H19ON has been isolated from the epigeal part ofN. schoberi and has been called… 
1967
1967
Chichibabin reaction. II. Chichibabin reaction of 8-methylquinoline and migration of the methyl group in the synthesis of 3,4-dihydro-8-methyl-carbostyril by friedel-crafts reaction. (Studies on the…
1947
1947
5-Hydroxyquinoline-8-carboxylic acid; a colorimetric reagent for ruthenium.
5-Aminoquinoline-8-carboxylic acid was prepared from 8-methylquinoline by nitration in the 5-position, oxidation of the methyl… 
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