Results 171 to 180 of about 4,015 (203)

Photochromism and thermochromism of Sn(IV) complexes with 8-aminoquinoline and salicylidene-8-aminoquinoline

Thermochimica Acta, 1994
Abstract Tin(IV) complexes with 8-aminoquinoline (complexes (1) and (2)) and with salicylidene-8-aminoquinoline (complex (3)) have been prepared and characterized. Complexes (1) and (3) are thermochromic, and display irreversible and reversible thermochromism, respectively.
Ahmed M. Donia, Hanaa El-Boraey
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Electrochemistry of ruthenium(ii) complexes of 8-aminoquinoline

Dalton Transactions, 2009
Oxidation of [Ru(NH(2)Q)(3)](2+) (NH(2)Q = 8-aminoquinoline) results in intermolecular coupling of 8-aminoquinoline ligands to yield an electroactive polymer. Oxidative polymerization is not observed for [Ru(bpy)(2)(NH(2)Q)](2+) (bpy = 2,2'-bipyridine), where only one 8-aminoquinoline ligand is present.
Megan K, O'Neill, Alfred Francois, Trappey, Paul, Battle, Christopher L, Boswell, David N, Blauch   +4 more
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Fluorescence and phosphorescence of 5- and 8-aminoquinoline

Analytica Chimica Acta, 1971
Abstract 5-Aminoquinoline and 8-aminoquinoline fluoresce moderately to weakly in low dielectric media but not in strongly hydrogen-bonding or acidic aqueous media. At low temperatures and in rigid media moderately intense fluorescence is observed in aqueous, media at all pH values.
S G, Schulman, L B, Sanders
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Remote C–H Functionalization of 8-Aminoquinoline Ring

Topics in Current Chemistry, 2020
8-Aminoquinoline is a common nitrogen-containing heterocyclic framework in many natural products, functional materials and useful drugs. It has been developed as a powerful bidentate directing group or ligand auxiliary in the field of C-H bond activation/functionalization in recent years.
Zhihui Xu, Xiaogang Yang, Shuang-Feng Yin, Renhua Qiu   +3 more
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8-Aminoquinolines: Primaquine and Tafenoquine

2011
8-Aminoquinolines are an important class of antimalarial drugs because they are effective against the liver stages of Plasmodium infections and thus are administered for radical cure and presumptive antirelapse therapy against relapsing malaria. In this chapter, we discuss two 8-aminoquinolines, primaquine and tafenoquine.
Norman C. Waters, Michael D. Edstein
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Synthesis of aminals from 8-aminoquinoline

Chemistry of Heterocyclic Compounds, 1981
The reaction of 8-aminoquinoline with substituted aromatic aldehydes leads to aminals, which are the only reaction products. The reaction with 1-formyl-2-hydroxynaphthalene proceeds with the formation of a Schiff base. The UV and mass spectra of the aminals are discussed.
N. S. Kozlov, G. V. Vorob'eva
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Reduced 8-aminoquinoline analogues as potential antimalarial agents

Journal of Medicinal Chemistry, 1976
The synthesis of 1-alkyl-8-(aminoalkylamino)-6-methyl1-1,2,3,4-tetrahydroquinolines, 8-(4'-amino-1'-methylbutylamino)-6-methoxy-1-methyl1-1,2-dihydroquinoline, 5-substituted 8-(4'-amino-1'-methylbutylamino)-1-methyl-1,2-dihydroquinolines, 8-alkylamino-1-(2-N,N-diethylaminoethyl)-6-methoxy-1,2,3,4-tetrahydroquinolines, 1-)2-N,N-diethylaminoethyl)-6 ...
F I, Carroll, J T, Blackwell, A, Philip, C E, Twine   +3 more
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Tafenoquine: A New 8- Aminoquinoline

Medical Journal of Zambia, 2012
No ...
Prashar, L, Paul, R
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Copper-Catalyzed Regioselective C–H Sulfonylation of 8-Aminoquinolines

The Journal of Organic Chemistry, 2016
Copper(I)-catalyzed 5-sulfonation of quinolines via bidentate-chelation assistance has been developed. The reaction is compatible with a wide range of quinoline substrates and arylsulfonyl chlorides. Experimental and theoretical (DFT) investigation implicated that a single-electron-transfer process is involved in this sulfonylation transformation.
Jun, Wei, Jingxing, Jiang, Xinsheng, Xiao, Dongen, Lin, Yuanfu, Deng, Zhuofeng, Ke, Huanfeng, Jiang, Wei, Zeng   +7 more
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Antimalarial Activity of Novel 5-Aryl-8-Aminoquinoline Derivatives

Journal of Medicinal Chemistry, 2010
In an attempt to separate the antimalarial activity of tafenoquine (3) from its hemolytic side effects in glucose-6-phosphate dehydrogenase (G6PD) deficiency patients, a series of 5-aryl-8-aminoquinoline derivatives was prepared and assessed for antimalarial activities.
Hiroaki, Shiraki, Michael P, Kozar, Victor, Melendez, Thomas H, Hudson, Colin, Ohrt, Alan J, Magill, Ai J, Lin   +6 more
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