Compounds > 1,10-phenanthroline

1,10-phenanthroline and 1-butanol

1,10-phenanthroline has been researched along with 1-butanol in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (80.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Keren, Z; LeGrue, SJ; Leland, F; Nakajima, M1
Leadbeater, NE1
Huang, K; Li, BJ; Li, H; Lu, XY; Shi, ZJ; Sun, CL; Yu, DG; Yu, M; Zheng, SF; Zhou, X1
Cuthbertson, J; Gray, VJ; Wilden, JD1
Jutand, A; Lei, A; Yi, H1

Other Studies

5 other study(ies) available for 1,10-phenanthroline and 1-butanol

ArticleYear
Inhibition of experimental metastasis and extracellular matrix degradation by butanol extracts from B16-F1 murine melanoma.
    Cancer research, 1989, Jan-15, Volume: 49, Issue:2

    Topics: 1-Butanol; Animals; Butanols; Cell Line; Chondroitin Sulfate Proteoglycans; Extracellular Matrix; Heparan Sulfate Proteoglycans; Heparin; Heparitin Sulfate; Melanoma; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Molecular Weight; Neoplasm Metastasis; Phenanthrolines

1989
Cross coupling: When is free really free?
    Nature chemistry, 2010, Volume: 2, Issue:12

    Topics: Butanols; Carbon; Catalysis; Mass Spectrometry; Palladium; Phenanthrolines; Transition Elements

2010
An efficient organocatalytic method for constructing biaryls through aromatic C-H activation.
    Nature chemistry, 2010, Volume: 2, Issue:12

    Topics: Bromides; Butanols; Carbon; Catalysis; Hydrogen; Iodides; Kinetics; Phenanthrolines; Transition Elements

2010
Observations on transition metal free biaryl coupling: potassium tert-butoxide alone promotes the reaction without diamine or phenanthroline catalysts.
    Chemical communications (Cambridge, England), 2014, Mar-11, Volume: 50, Issue:20

    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.
    Chemical communications (Cambridge, England), 2015, Jan-11, Volume: 51, Issue:3

    Topics: Anions; Bromides; Butanols; Catalysis; Electrons; Free Radicals; Molecular Structure; Oxidation-Reduction; Phenanthrolines

2015