Tetrahydroquinoline

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Tetrahydroquinoline

Tetrahydroquinoline is an organic compound that is the semi-hydrogenated derivative of quinoline. It is a colorless oil. Substituted derivatives of tetrahydroquinoline are common in medicinal chemistry. Tetrahydroquinolines are produced by hydrogenation of quinolines. Because the hydrogenation is reversible, tetrahydroquinoline has been often examined as a hydrogen-donor solvent in coal liquifaction. Using homogeneous catalysts , asymmetric hydrogenation has been demonstrated. Contents move to sidebar hide. Article Talk. Read Edit View history. Tools Tools. Download as PDF Printable version. CAS Number. Interactive image. Beilstein Reference.

A ligand- and base-free silver-catalyzed reduction tetrahydroquinoline quinolines provides a facile, tetrahydroquinoline, environmentally friendly, and practical access to various 1,2,3,4-tetrahydroquinoline derivatives at room temperature. Some documentation and label information may refer to the legacy brand.

Xiong, S. Li, B. Fu, J. Wang, Q. Wang, W. Yang, Org.

Federal government websites often end in. The site is secure. A review of the recent literature is given focusing on synthetic approaches to 1,2,3,4-tetrahydroquinolines, 2,3-dihydro-4 1 H -quinolinones and 4 1 H -quinolinones using domino reactions. These syntheses involve: 1 reduction or oxidation followed by cyclization; 2 S N Ar-terminated sequences; 3 acid-catalyzed ring closures or rearrangements; 4 high temperature cyclizations and 5 metal-promoted processes as well as several less thoroughly studied reactions. Each domino method is presented with a brief discussion of mechanism, scope, yields, simplicity and potential utility. Domino reactions, also known as tandem or cascade reactions, have emerged as a highly effective strategy for the synthesis of bioactive natural products and pharmaceutical agents [ 1 ]. These methods enable chemists to perform complex synthetic conversions with high efficiency using simple starting materials, often via a biomimetic pathway [ 2 ].

Tetrahydroquinoline

Tetrahydroquinoline is an organic compound that is the semi-hydrogenated derivative of quinoline. It is a colorless oil. Substituted derivatives of tetrahydroquinoline are common in medicinal chemistry. Tetrahydroquinolines are produced by hydrogenation of quinolines. Because the hydrogenation is reversible, tetrahydroquinoline has been often examined as a hydrogen-donor solvent in coal liquifaction. Using homogeneous catalysts , asymmetric hydrogenation has been demonstrated. Contents move to sidebar hide.

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View All Antibodies. Zhu, J. PCR Plates. Social activity. Adhikari, D. Cong, X. Google Analytics. Nature , Liu, X. Jump to site search. Statistics 1 Statistics Statistics cookies collect information anonymously. View All Cell Culture. Research Use Only! Because the hydrogenation is reversible, tetrahydroquinoline has been often examined as a hydrogen-donor solvent in coal liquifaction.

Xiong, S. Li, B. Fu, J.

Adhikari, D. PMID An environmentally friendly iridium-catalyzed direct cyclization of N -methylanilines with 1,3-propanediol provides tetrahydroquinolines with water as the sole by-product. Download as PDF Printable version. Antibodies Advanced Search. Tetrahydroquinolines are produced by hydrogenation of quinolines. CAS Google Scholar. Chen, S. Show More Show Less. Tu, Z. Bhattacharyya, S. The use of NaBH 4 or DDQ in a subsequent step enables the synthesis of tetrahydroquinolines or quinolines, respectively. Cancel missing translation for 'submit'. Some of them are essential, while others help us to improve this website and your experience. Don't have a profile?