110545-79-4Relevant articles and documents
Intramolecular transaminations of enaminones: A synthesis of fused, polycyclic, N-aryl pyridones
Friary,Seidl,Schwerdt,Cohen,Hou,Nafissi
, p. 7169 - 7178 (1993)
2-Arylamino-3-pyridinecarbonyl chlorides acylated the β-carbon atoms of enamines, and the resulting enaminones cyclized to give a series of fused polycyclic N-aryl pyridones. The series included 10-(3-chlorophenyl)-6,8,9,10-tetrahydrobenzo[b][1,8]naphthyr
The chemical reactivity of a known anti-psoriasis drug. Part 1: Further insights into the products resulting from oxidative cleavage
Jones, Alan M.,Lorion, Magali M.,Lebl, Tomas,Slawin, Alexandra M.Z.,Philp, Douglas,Westwood, Nicholas J.
, p. 9667 - 9674 (2010)
The oxidative cleavage of the known anti-psoriasis drug 1 to give 2 has been reported previously. Due to the importance of accessing medium-sized ring containing systems via oxidative cleavage, this reaction has been revisited revealing additional informa
Synthesis and characterisation of medium-sized ring systems by oxidative cleavage. Part 2: Insights from the study of ring expanded analogues
Lebl, Tomas,Lorion, Magali M.,Jones, Alan M.,Philp, Douglas,Westwood, Nicholas J.
experimental part, p. 9694 - 9702 (2011/02/23)
Variable temperature NMR analysis and computational methods have been used to develop a detailed understanding of the 1H NMR spectra of a family of medium-sized ring containing compounds. The family consists of analogues containing 10-, 11- and
Intermolecular Transaminations of Enaminones: A Synthesis of Fused, Polycyclic, N-Aryl Pyridones
Friary, Richard J.,Seidl, Vera,Schwerdt, John H.,Chan, Tze-Ming,Cohen, Marvin P.,et al.
, p. 7179 - 7192 (2007/10/02)
Aryl amines reacted with enaminones like (2-chloro-3-pyridinyl)methanone, and the transaminated products cyclized to aryl-substituted pyridones like 6,7,8,9-tetrahydro-9-phenyl-5H-cyclopentanaphthyridin-5-one
Polycyclic quinoline, naphthyridine and pyrazinopyridine derivatives
-
, (2008/06/13)
Novel polycyclic quinoline, naphthyridine and pyrazinopyridine derivatives are disclosed which are useful for treating allergic reactions, inflammation, peptic ulcers, hypertension, and hyperproliferative skin diseases and for suppressing the immune respo