1046136-16-6Relevant academic research and scientific papers
A simple and efficient copper-catalyzed synthesis of N-alkynylimidazoles
Wang, Man-Gang,Wu, Jun,Shang, Zhi-Cai
supporting information; experimental part, p. 589 - 594 (2012/03/27)
A simple and efficient method for the synthesis of N-alkynylheteroarenes from 1,1-dibromo-1-alkenes was developed via a copper-catalyzed cross-coupling reaction. Generally superior yields and functional-group tolerance were obtained with TMEDA as ligand using imidazole and benzimidazole substrates in dioxane. Georg Thieme Verlag Stuttgart · New York.
Copper-catalyzed coupling of imidazoles and pyrazoles with 1,1-dibromo-1-alkenes: A distinct approach for direct N-alkynylation of heteroarenes
Das, Biswanath,Salvanna,Reddy, Gandolla Chinna,Balasubramanyam, Penagaluri
experimental part, p. 6497 - 6500 (2011/12/15)
The direct N-alkynylation of heteroarenes, imidazoles, and pyrazoles with 1,1-dibromo-1-alkene has been carried out for the first time using [Cu(Phen)PPh3Br] (as a catalyst) and Cs2CO3 in DMSO at 80 °C. The products are formed in good to high yields (66-85%) within 3 h. No side products could be detected.
Copper(II) oxide catalyzed ligand-free coupling reaction of heteroarenes with bromoalkynes
Das, Biswanath,Reddy, Gandolla Chinna,Balasubramanyam, Penagaluri,Salvanna
experimental part, p. 816 - 820 (2011/04/25)
The coupling reaction of imidazoles and pyrazoles with bromoacetylenes has efficiently been carried out under ligand-free conditions in the presence of copper(II) oxide as the catalyst using potassium hydroxide in 1,4-dioxane at 80 C. The method is a simpler access to N-alk-1-ynyl- and/or N-(2-bromovinyl)- substituted heteroarenes. Georg Thieme Verlag Stuttgart New York.
Cu-catalyzed N-alkynylation of imidazoles, benzimidazoles, indazoles, and pyrazoles using PEG as solvent medium
Burley, Glenn A.,Davies, David L.,Griffith, Gerry A.,Lee, Michael,Singh, Kuldip
supporting information; experimental part, p. 980 - 983 (2010/05/18)
(Chemical Equation Presented) A facile and efficient Cu(I)-catalyzed cross-coupling method is reported for the preparation of N-alkynyl or N-bromoalkenyl heteroarenes from bromoalkynes. Generally superior yields and functional group tolerance were obtained with microwave (MW) irradiation using imidazole, benzimidazole, pyrazole, and indazole substrates and poly(ethylene glycol) 400 (PEG400) as an additive. We speculate that PEG400 acts as both a Cu(I)-stabilizing ligand as well as a phase transfer solvent.
Lithiation and functionalization of 1-alkynylimidazoles at the 2-position
Laroche, Christophe,Kerwin, Sean M.
experimental part, p. 5194 - 5197 (2009/12/06)
Functionalization reactions of 1-alkynylimidazoles involving the formation of their 2-lithio derivatives followed by addition of various electrophiles are presented. This allows access to previously unreported 1,2-dialkynylimidazoles via 1-alkynyl-2-iodoi
Coupling reactions of bromoalkynes with imidazoles mediated by copper salts: Synthesis of novel N-alkynylimidazoles
Laroche, Christophe,Li, Jing,Freyer, Matthew W.,Kerwin, Sean M.
, p. 6462 - 6465 (2008/12/22)
(Chemical Equation Presented) A cross-coupling reaction of imidazoles with bromoalkynes in the presence of a catalytic amount of CuI is reported. This protocol allows an access to novel N-(1-alkynyl)imidazoles in moderate to good yields.
