110546-46-8Relevant articles and documents
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.
supporting information; scheme or table, 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
Intramolecular transaminations of enaminones: A synthesis of fused, polycyclic, N-aryl pyridones
Friary,Seidl,Schwerdt,Cohen,Hou,Nafissi
, p. 7169 - 7178 (2007/10/02)
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
