1,7-phenanthroline has been researched along with tert-butoxide, potassium in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Leadbeater, NE | 1 |
| Huang, K; Li, BJ; Li, H; Lu, XY; Shi, ZJ; Sun, CL; Yu, DG; Yu, M; Zheng, SF; Zhou, X | 1 |
| Gu, YF; Huang, WP; Shi, ZJ; Sun, CL | 1 |
| Cuthbertson, J; Gray, VJ; Wilden, JD | 1 |
| Jutand, A; Lei, A; Yi, H | 1 |
5 other study(ies) available for 1,7-phenanthroline and tert-butoxide, potassium
| Article | Year |
|---|---|
Cross coupling: When is free really free?
Topics: Butanols; Carbon; Catalysis; Mass Spectrometry; Palladium; Phenanthrolines; Transition Elements | 2010 |
An efficient organocatalytic method for constructing biaryls through aromatic C-H activation.
Topics: Bromides; Butanols; Carbon; Catalysis; Hydrogen; Iodides; Kinetics; Phenanthrolines; Transition Elements | 2010 |
Neocuproine-KOtBu promoted intramolecular cross coupling to approach fused rings.
Topics: Butanols; Hydrocarbons, Aromatic; Phenanthrolines | 2011 |
Observations on transition metal free biaryl coupling: potassium tert-butoxide alone promotes the reaction without diamine or phenanthroline catalysts.
Topics: Butanols; Catalysis; Diamines; Magnetic Resonance Spectroscopy; Molecular Structure; Phenanthrolines; Transition Elements | 2014 |
Evidence for the interaction between (t)BuOK and 1,10-phenanthroline to form the 1,10-phenanthroline radical anion: a key step for the activation of aryl bromides by electron transfer.
Topics: Anions; Bromides; Butanols; Catalysis; Electrons; Free Radicals; Molecular Structure; Oxidation-Reduction; Phenanthrolines | 2015 |