22 research outputs found
(20S,2âČâČS)-20-[4âČ-(3âČâČ-Hydroxy-2âČâČ-methylÂpropÂyl)-3âČ-methylisoxazol-5-yl]-5ÎČ-pregÂnan-3ÎČ,16ÎČ-diol
The title steroidal compound, C29H47NO4, was prepared in a one-pot reaction starting from a sarsasapogenin derivative of known configuration. The isoxazole heterocycle is oriented towards the α face of the steroid nucleus and, although fully functionalized on C atoms, does not provoke steric hindrance with the adjacent D ring. The absolute configuration observed for chiral centers is as expected, and shows that no epimerization occurred in the precursors. In the crystal, the three OH groups serve as donors for hydrogen bonding with O and N atoms. The isoxazole N atom is involved in OâHâŻN hydrogen bonds, forming chains along [100]. These chains are further connected via OâHâŻO and weak CâHâŻO contacts, giving rise to a three-dimensional supraÂmolecular network
The zwitterion (23âČE)-(23R,25S)-23-[1-(oxidoiminio)ethÂyl]-5ÎČ-spiroÂstan-3ÎČ-yl acetate
The title steroidal compound, C31H49NO5, resulted from the selective oximation of (23R)-23-acetylÂsarsasapogenin acetate. One- and two-dimensional 1H and 13C NMR spectra, as well as IR data, are in agreement with the presence of a ketoxime group at C-23. However, recrystallization in slightly acidic media affords the title compound in the rare zwitterionic oxime form, as a consequence of migration of the hydrÂoxy H atom to the N atom in the oxime group. This H atom is clearly detected and its position was refined from X-ray data. The geometry for the C=N+(H)âOâ group features long C=N and short NâO bond lengths compared to non-zwitterionic oximes. The ketoxime is stabilized with the E configuration, avoiding steric hindrance between the oxime O atom and H atom at C-23. The sum of the angles around the oxime N atom is 359.6°, giving a planar configuration for that atom, as expected for sp
2 hybridization
(R)-1-PhenylÂethylÂammonium trifluoroÂacetate
In the crystal structure of the title salt, C8H12N+·C2F3O2
â, all of the ammonium H atoms serve as donors for hydrogen bonds to carboxylÂate O atoms, forming an R
4
3(10) ring motif based on two cations and two anions. Since both cations and anions act as inter-ion bridging groups, R(10) rings aggregate in a one-dimensional supraÂmolecular network by sharing the strongest NâHâŻO bond. Edge-sharing motifs lie on the twofold screw axis parallel to [010], and antiÂparallel packing of these 21-column structural units results in the crystal structure. This arrangement is one of the most commonly occurring in conglomerates of chiral 1-phenylÂethylÂamine with achiral monocarboxylic acids, confirming that these ionic salts are particularly robust supraÂmolecular heterosynthons useful in crystal engineering
(E)-(25S)-23-Acetyl-5ÎČ-furost-22-ene-3ÎČ,26-diol
The title steroid, C29H46O4, is a furostene derivative with a C=C double-bond length of 1.353â
(3)â
Ă
and an E configuration. The side chain is oriented toward the α face of the AâE steroidal nucleus and presents a disordered terminal CH2âOH group [occupancies for resolved sites are 0.591â
(9) and 0.409â
(9)]. The methyl group at C20 attached to ring E is also oriented toward the α face, avoiding steric hindrance with the carbonyl O atom of the acetyl group. The furostene and acetyl functionalities form an α,ÎČ-unsaturated ketone system, with an s-cis configuration. All hydrÂoxy and carbonyl groups are involved in weak interÂmolecular hydrogen bonds. The absolute configuration was assigned from the synthesis
Retos actuales de la farmacia
Retos actuales de la farmacia es un proyecto que estĂĄ coordinado por Leobargo Manuel GĂłmez OlivĂĄn y un equipo de investigadores que forman parte del claustro de la Facultad de QuĂmica en el ĂĄrea de posgrado, ellos han incentivado el espĂritu investigador y cientĂfico de los estudiantes adscritos al programa para adentrarse en el ĂĄmbito farmacĂ©utico. Los capĂtulos que conforman esta ediciĂłn son el reflejo de la actividad acadĂ©mica desarrollada en este posgrado en las diferentes ĂĄreas de acentuaciĂłn que lo conforman: farmacia molecular, farmacia social y tecnologĂa farmacĂ©utica
Mis casos clĂnicos de especialidades odontolĂłgicas
Libro que muestra la atenciĂłn de casos clĂnicos particulares referente a las diferentes especialidades odontolĂłgicasLibro que muestra la atenciĂłn de casos clĂnicos particulares referente a las diferentes especialidades odontolĂłgicasUniversidad AutĂłnoma de Campeche
Universidad AutĂłnoma del Estado de Hidalgo
Universidad AutĂłnoma del Estado de MĂ©xic
SĂntesis enantiopura de cetoiminas y diiminas quirales a partir de derivados furostĂ©nicos
IntervenciĂłn psicoeducativa: una propuesta para fomentar la asertividad en adolescentes de 1er. grado de secundaria
Licenciatura en PsicologĂa Educativ