Tetrahydroquinoline

Xiong, S.

Products Items of N- 1,2,3,4-Tetrahydroquinolinecarbonothioyl benzamide. TM Get our latest updates. We use cookies on our website. Some of them are essential, while others help us to improve this website and your experience.

Tetrahydroquinoline

Don't have a profile? This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. No offer available. Gel Electrophoresis Equipment and Supplies. View All Antibodies. Antibodies Advanced Search. Biochemicals and Reagents. Biological Buffers. Custom Services and Products. Enzymes and Inhibitors.

Chen, H.

JavaScript seems to be disabled in your browser. You must have JavaScript enabled in your browser to utilize the functionality of this website. Chem Service, Inc. West Chester, PA Email to a Friend. Be the first to review this product.

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.

Tetrahydroquinoline

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 ]. Thus, domino reactions contribute immensely to synthetic drug design strategies, enhance aesthetic approaches in total synthesis, and improve yields in large-scale synthesis [ 1 , 2 ].

No te fuiste del todo frases

Gandhamsetty, S. Cell Based Assays. A three-component Povarov reaction of aldehydes, anilines, and benzyl N -vinylcarbamate in the presence of 0. Description This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Wang, W. Espinosa, H. Statistics 1 Statistics Statistics cookies collect information anonymously. Tubes and Bottles. Luo, X. View All Protein Biology. Chen, H. Zhu, J. Download references. Other names Hydroquinoline. Using homogeneous catalysts , asymmetric hydrogenation has been demonstrated.

Xiong, S. Li, B.

Akiyama, H. Statistics cookies collect information anonymously. Patel, D. Skip to main content Thank you for visiting nature. Chen, L. Das, Org. Recombinant Proteins Recombinant Proteins. Minakawa, K. Trusted Sustainability Partner Suppliers who meet our established requirements for corporate social responsibility. Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily. Chen, N. Fujita, L. Wu, P. Beilstein Reference. Hu, X.