4015-24-1Relevant academic research and scientific papers
Scaled-up transition-metal-catalyzed cross-coupling reactions of thioether-substituted N-heterocycles with organozinc reagents
Metzger, Albrecht,Melzig, Laurin,Knochel, Paul
experimental part, p. 2853 - 2858 (2010/10/03)
A variety of functionalized methylthio-substituted N-heterocycles (pyridines, pyrimidines, pyrazines, pyridazines, triazines, quinazolines, benzothiazoles) undergo smooth palladium- or nickel-catalyzed cross-couplings with highly functionalized organozinc reagents at ambient temperature. No expensive copper(I) salts are required and the coupling reactions proceed readily in the range of up to 20 mmol scale. Georg Thieme Verlag Stuttgart.
Molecular design and synthesis of 4,8-di(hetero)arylquinazolines with potential applications in quadratic nonlinear oprics. Diazines part 48
Busch, Alexandrine,Turck, Alain,Nowicka, Kamila,Barsella, Alberto,Andraud, Chantal,Plé, Nelly
, p. 1723 - 1741 (2008/03/14)
In the aim to define a structure NLO properties relationship, theoretical calculations have been used to investigate the role of different parts (substituents and π-system) of disubstituted conjugated systems based on naphthalene, cinnoline and quinazolin
Synthesis of 4,8-diarylcinnolines and quinazolines with potential applications in nonlinear optics. Diazines. Part 28
Gautheron Chapoulaud,Plé,Turck,Quéguiner
, p. 5499 - 5507 (2007/10/03)
New 4,8-diarylbenzodiazines have been synthesized using cross-coupling reactions and regioselective metalation at the peri-position C8 of the benzene moiety of various cinnolines and quinazolines. Some of these compounds have been tested to assess their nonlinear optical properties. (C) 2000 Elsevier Science Ltd.
