Vladimir Carranza-Téllez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Vladimir Carranza-Téllez has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- A. Cortes Santiago
Centro de Investigación en Dispositivos Semiconductors, del Instituto de Ciencias de la Universidad Autónoma de Puebla, Av. 14 Sur Col Jardines de San Manuel, Ciudad Universitaria, Puebla, Puebla, 72000, Mexico
1 shared publication - Alan Carrasco-Carballo
Laboratorio de Elucidación y Síntesis en Química Orgánica, Centro de Química, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Puebla 72570, Mexico
1 shared publication - H. Azucena Coyotecatl
Fac. de Ciencias de la Electrónica, Universidad Autónoma de Puebla, Pue., P.O. Box 1067, C.P. 72001, Mexico
1 shared publication - Hisami Rodriguez-Matsui
Laboratorio de Elucidación y Síntesis en Química Orgánica, Centro de Química, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Puebla 72570, Mexico
1 shared publication - Héctor Juárez
Benemérita Universidad Autónoma de Puebla
1 shared publication - J. Luis Sánchez-Juárez
Laboratorio de Elucidación y Síntesis en Química Orgánica, Centro de Química, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Puebla 72570, Mexico
1 shared publication
Latest Publications
- Open Access
Synthesis of a New Bioconjugate Steroid Pyridinium Salt Derived from Allopregnanolone Acetate
Because allopregnanolone and derivatives represent biologically active molecules, in this letter, we present the synthesis of a new bioconjugate steroid pyridinium salt derived from allopregnanolone in three steps. The key steps involve the formation of the hydrazone intermediate, followed by condensation with bromoacetyl bromide and subsequent coupling with pyridine to generate the pyridinium bromide salt. The new bioconjugate steroid pyridinium salt, 4, was fully characterized by proton and carbon nuclear magnetic resonance (1H and 13C NMR) spectroscopy, mass spectrometry (MS), and Fourier transform infrared spectroscopy (FTIR). 1H-NMR analysis revealed the presence of a dynamic rotameric mixture in a 7:3 ratio of Z/E amide conformers, which were identified by a 2D NOESY experiment.
Open AccessSynthesis of a New Bioconjugate Steroid Pyridinium Salt Derived from Allopregnanolone Acetate
Because allopregnanolone and derivatives represent biologically active molecules, in this letter, we present the synthesis of a new bioconjugate steroid pyridinium salt derived from allopregnanolone in three steps. The key steps involve the formation of the hydrazone intermediate, followed by condensation with bromoacetyl bromide and subsequent coupling with pyridine to generate the pyridinium bromide salt. The new bioconjugate steroid pyridinium salt, 4, was fully characterized by proton and carbon nuclear magnetic resonance (1H and 13C NMR) spectroscopy, mass spectrometry (MS), and Fourier transform infrared spectroscopy (FTIR). 1H-NMR analysis revealed the presence of a dynamic rotameric mixture in a 7:3 ratio of Z/E amide conformers, which were identified by a 2D NOESY experiment.
- 24 December 2020
- Published by Elsevier in Optical Materials
- Vol. 112, 110747
Green synthesis of palladium mixed with PdO nanoparticles by chemical bath deposition
- 24 December 2020
- Published by Elsevier in Optical Materials
- Vol. 112, 110747
Green synthesis of palladium mixed with PdO nanoparticles by chemical bath deposition