Chemistry Heterocyclic Building Blocks Tetrahydroquinolines
An organic compound known as tetrahydroquinoline, which is a partially hydrogenated form of quinoline, exists as a colorless oil.
Quinolines can be hydrogenated to produce tetrahydroquinolines, which are commonly studied as a hydrogen-donor solvent in coal liquefaction due to the reversible nature of the hydrogenation process.
1,2,3,4-Tetrahydroquinoline serves as an antioxidant and corrosion inhibitor, and also functions as an active ingredient in several dyes.
Medicinal chemistry often utilizes substituted derivatives of tetrahydroquinoline, which include bioactive compounds such as oxamniquine, dynemycin, viratmycin, and nicainoprol.
Heterogeneous catalysts are typically used to prepare tetrahydroquinoline derivatives through the hydrogenation of the corresponding quinoline.
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1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroquinoline-7-carboxylic acid
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7-(4-Chlorobutoxy)-3,4-dihydroquinolin-2(1H)-one
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6-Bromo-4-methyl-1,2,3,4-tetrahydroquinoline
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3-Amino-1-methyl-3,4-dihydroquinolin-2(1H)-one
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one
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6-(tert-Butyl)-3,4-dihydroquinolin-2(1H)-one
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1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one
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8-Amino-3,4-dihydroisoquinolin-1(2H)-one
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6-Amino-8-fluoro-3,4-dihydroquinolin-2(1H)-one
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6-Bromo-2-oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid
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Methyl 2-methoxy-6-oxo-5,6,7,8-tetrahydroquinoline-5-carboxylate
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6-Bromo-1-methyl-3,4-dihydroquinolin-2(1H)-one
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1,2,3,4-Tetrahydroquinoline-7-carboxylic acid
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1-Ethyl-6-fluoro-1,2,3,4-tetrahydroquinoline