Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Homar S. Barcena"'
Autor:
Homar S. Barcena, Katarzyna Maziarz
Publikováno v:
Journal of Chemical Education. 94:1538-1542
In an effort to repurpose expired guaifenesin tablets, experiments devised for practical instruction are reported for the preparation and isolation of the guaifenesin acetonide using a microscale kit. The laboratory experiment successfully utilizes a
Publikováno v:
Journal of Chemical Education. 94:1314-1318
The synthesis of epoxidized soybean oil (ESO) provides students a vantage point on the application of green chemistry principles in a series of experiments. Qualitative tests review the reactions of alkenes, whereas spectroscopic analyses provide ins
Autor:
Peishan Chen, Homar S. Barcena
Publikováno v:
Journal of Chemical Education. 93:202-205
Students are introduced to spectrophotometry in comparing the antioxidant activity of pure eugenol and oil of cloves from a commercial source using a modified ferric reducing antioxidant power (FRAP) assay. The extraction of the essential oil from dr
Autor:
Jodie T. Fahey, Lynn E. Maelia, J. Fahey, L. Maelia, Barbora Morra, Andrew P. Dicks, V. Fishback, B. Reid, A. Schildkret, Loyd D. Bastin, Kaitlyn Gerhart, E. M. Gross, S. H. Williams, E. Williams, D. A. Dobberpuhl, J. Fujita, J. T. Fahey, A. E. Dineen, J. M. Henain, Renuka Manchanayakage, Grant W. Fahnhorst, Zachary J. Swingen, Deborah K. Schneiderman, Christa S. Blaquiere, Michael T. Wentzel, Jane E. Wissinger, Homar S. Barcena
Autor:
Homar S. Barcena
Publikováno v:
ACS Symposium Series ISBN: 9780841231771
ACS Symposium Series
ACS Symposium Series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8664f19676b7f2e3adb91475bd29b72c
https://doi.org/10.1021/bk-2016-1233.ch009
https://doi.org/10.1021/bk-2016-1233.ch009
Publikováno v:
SpringerPlus
Anthocyanidins were synthesized to study the effect of methoxy substitution on the B ring to their antioxidant property. Comparative FRAP studies show 2′- and 4′-methoxy substituents have higher antioxidant activities, which may be attributed to
Publikováno v:
Inorganic chemistry. 44(21)
Previously, we reported the synthesis and preliminary characterization of Cu(I/II) complexes of N,N-bis(2-quinilylmethyl)-(l)-methionine (Zahn, S.; Canary, J. W. Science 2000, 288, 1404-7). The chemically oxidized and reduced forms of the complexes g
Publikováno v:
Organic letters. 5(5)
One-electron reduction inverts the helicity of copper complexes formed from derivatives of S-methylcysteine and methioninol. The change in conformation of the organic ligand is followed in the exciton-coupled circular dichroism (ECCD) spectra of the