509078-07-3Relevant articles and documents
Selective Synthesis of Hetero-Sequenced Aza-Cyclophanes
Otte, Matthias,Lutz, Martin,Klein Gebbink, Robertus J. M.
, p. 1657 - 1661 (2017)
The selective synthesis of purely organic cages with hetero-sequenced functionalized cavities is demonstrated. The strategy to obtain these compounds is based on a stepwise approach using thermodynamically controlled imine condensations. To accomplish thi
A pyridine based: Meta -linking deep-blue emitter with high conjugation extent and electroluminescence efficiencies
Zhu, Ze-Lin,Chen, Wen-Cheng,Zhang, Liang-Dong,Liu, Xiao-Le,Tong, Qing-Xiao,Wong, Fu-Lung,Lu, Feng,Lee, Chun-Sing
, p. 6249 - 6255 (2016)
We designed and synthesized a bipolar deep-blue emitter 2,6-bis(4-(1-(4-(tert-butyl)phenyl)-1H-phenanthro[9,10-d]imidazol-2-yl)phenyl)pyridine (26BTPIPy) based on a meta-linking D-π-A-π-D structure. Compared to its para-linking analogue (25BTPIPy), the me
Carboxyamido/carbene ligated palladium (II) complex: A versatile catalyst for the synthesis of aryl-substituted heteroarenes
Vishnuvardhan Reddy, Police,Parsharamulu, Thupakula,Annapurna, Manne,Likhar, Pravin R.,Kantam, Mannepalli Lakshmi,Bhargava, Suresh
supporting information, p. 150 - 153 (2016/12/06)
Carboxy amido/carbene ligated Pd-complex catalyzed Suzuki-Miyaura cross-coupling of aryl-boronic acids with heteroaryl bromides is described. The protocol has a broad substrate scope that includes electron-rich, electron-deficient and sterically hindered arylboronic acids and heteroaryl bromides. The catalytic activity of the catalyst has been further investigated in the coupling of 2,6-dibromopyridine with arylboronic acids.
Bioimaging, antibacterial and antifungal properties of imidazole-pyridine fluorophores: Synthesis, characterization and solvatochromism
Nagarajan,Vanitha,Ananth, D. Arul,Rameshkumar,Sivasudha,Renganathan
, p. 212 - 222 (2013/10/08)
A series of imidazole derivatives connected with pyridine moiety through phenyl groups were synthesized by using Suzuki coupling followed by multicomponent cyclization reaction. Results obtained from spectroscopic ( 1H NMR, 13C NMR,
Synthesis of chiral nonracemic polyimine macrocycles from cyclocondensation reactions of biaryl and terphenyl aromatic dicarboxaldehydes and 1R,2R-diaminocyclohexane
Kuhnert, Nikolai,Patel, Chirag,Jami, Fatemeh
, p. 7575 - 7579 (2007/10/03)
The synthesis of biaryl and terphenyl dicarboxaldehydes using Suzuki coupling methodology and their macrocyclisation reactions with 1R,2R-diaminocyclohexane yielding novel polyimine macrocycles derived from the [2+2] and [3+3] cyclocondensation reactions
