Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Amira Khaled"'
Autor:
Amira, Khaled1 (AUTHOR) kamira@sbu.edu, Muzere, Mark L.2 (AUTHOR) markmuzere@gmail.com
Publikováno v:
Review of Pacific Basin Financial Markets & Policies. Jun2024, Vol. 27 Issue 2, p1-10. 10p.
Publikováno v:
In Journal of Financial Stability October 2016 26:78-89
Publikováno v:
In Journal of Corporate Finance September 2013 22:209-220
Publikováno v:
The CASE Journal, 2010, Vol. 7, Issue 1, pp. 19-47.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/TCJ-07-2010-B003
Publikováno v:
In Journal of International Money and Finance 2011 30(6):1234-1263
Publikováno v:
Journal of Molecular Structure. 1263:133003
Autor:
Malika Berredjem, Mekki Kadri, Dounia Guibedj, Amira Khaled, Hocine Akkari, Hadjer Bougherara
Publikováno v:
Journal of Molecular Structure. 1202:127190
Interactions of methoxyphenyl N-sulfamoyloxazolidinone (SOZ) with Cu(II) and Co(II) ions in ethanol at 25 °C were studied experimentally using UV–Vis spectrophotometry. The data processing with a nonlinear least square fitting allowed the determin
Autor:
Amira, Khaled1 amira@cua.edu
Publikováno v:
Journal of Business Finance & Accounting. Jun/Jul2004, Vol. 31 Issue 5/6, p795-821. 27p. 7 Charts, 2 Graphs.
Autor:
Andrea Caprini, Daniele Lecis, Ilaria Motto, Amira Khaled, Cristina Battaglia, Martino Bolognesi, Francesca Vasile, Aldo Bianchi, Federica Cossu, Federica Servida, Moira Marizzoni, Elena de Franco, Pierfausto Seneci, Vincenzo Rizzo, Carmelo Drago, Leonardo Manzoni, Donatella Potenza, Marilenia De Matteo, Elisa Turlizzi, Mario Milani, Domenico Delia, Elisabetta Moroni, Eloise Mastrangelo, Maurizio Varrone, Laura Belvisi, Carlo Scolastico
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:5834-5856
Novel proapoptotic Smac mimics/IAPs inhibitors have been designed, synthesized and characterized. Computational models and structural studies (crystallography, NMR) have elucidated the SAR of this class of inhibitors, and have permitted further optim
Publikováno v:
Tetrahedron: Asymmetry. 18:2121-2124
An efficient synthesis of di-mannosyl serinyl phosphate using a convergent strategy involving a silver assisted nucleophilic substitution of tetra- O -acetyl-α- d -mannopyranosyl bromide by a conveniently protected O -serinyl phosphate is described.