J. Luis Sánchez-Juárez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
J. Luis Sánchez-Juárez has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- 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 - 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 - Jesús Sandoval-Ramírez
Laboratorio de Modificación y síntesis en Productos Naturales, Facultad de Ciencias Químicas, BUAP, Puebla 72570, Mexico
1 shared publication - Joel L. Terán
Centro de Quimica, Instituto de Ciencias, BUAP, Puebla 72570, Mexico
1 shared publication - Vladimir Carranza-Téllez
Centro de Quimica, Instituto de Ciencias, BUAP, 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.