150514-48-0Relevant academic research and scientific papers
Nickel(0)/NaHMDS adduct-mediated intramolecular alkylation of unactivated arenes via a homolytic aromatic substitution mechanism
Beaulieu, Louis-Philippe B.,Roman, Daniela Sustac,Vallee, Frederic,Charette, Andre B.
supporting information; experimental part, p. 8249 - 8251 (2012/09/07)
A variety of polycycles can be synthesized via an intramolecular alkylation cyclization promoted by Ni(PPh3)4 and NaHMDS. Mechanistic investigations support the catalytic nature of Ni0 in the course of TEMPO scavenging experiments and its association with the substrate and NaHMDS to form an adduct by DOSY NMR.
N-substituted aminoquinolines as analgesic agents
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, (2008/06/13)
There are disclosed compounds of the formula STR1 wherein R is hydrogen, halo or trifluoromethyl;R 1 is hydrogen or X;R 2 is hydrogen or X; with the proviso that when R 1 is X, R 2 is hydrogen, and when R 1 is hydrogen, R 2 is X;X is the moiety STR2 where
