Tetrahydroquinoline

Don't have a profile? This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product tetrahydroquinoline. Some documentation and label information may refer to the legacy brand, tetrahydroquinoline.

Maurya, O. Patel, D. Anand and P. Yadav, Org. To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page. If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

Tetrahydroquinoline

Thank you for visiting nature. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser or turn off compatibility mode in Internet Explorer. In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. IN connexion with work on tetrahydroquinoline derivatives of medicinal interest, we have recently synthesized a number of alkoxy- and alkyl-substituted 1,2,3,4-tetrahydroquinolines 1 in which various dialkylaminoalkyl groups carrying in some cases heterocyclic residues such as morpholino, piperidino, etc. Among the compounds tested so far, N -[2- 4-morpholino ethyl]1,2,3,4-tetrahydroquinoline I has shown interesting biological activity. Aisha Y. Hassan, Sara N. Shabaan, … Eman S. Thyagarajan, G. Kacker, I. CAS Google Scholar.

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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 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.

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.

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In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. View return policy. New Potent Tetrahydroquinoline Derivative. Hu, X. Accept All Save. Chem Service, Inc. Questions: There are no product questions yet. Categories : Amine solvents Tetrahydroquinolines. Using homogeneous catalysts , asymmetric hydrogenation has been demonstrated. To receive the discount customers must purchase three of the same product at list price in a single order to receive Patel , a Devireddy Anand a and Prem P. Statistics 1 Statistics. We Set The Standard. Weighing Papers and Dishes. Infobox references.

Xiong, S. Li, B.

Retailleau, J. Senapati, A. Article type Research Article. Han, L. Carlos Wang, Q. Anyone you share the following link with will be able to read this content:. Search Search articles by subject, keyword or author. Yu, M. Nandi, P. Statistics 1 Statistics.