Farrah Cañavera-Buelvas

Dr. Farrah Cañavera-Buelvas

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Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 June 2011 in Organometallics
Verified
Journal Article
Closed access
ARAdán Reyes-Sánchez
Adán Reyes-Sánchez
FCFarrah Cañavera-Buelvas
Farrah Cañavera-Buelvas
RBRigoberto Barrios-Francisco
Rigoberto Barrios-Francisco
OCOlga L. Cifuentes-Vaca
Olga L. Cifuentes-Vaca
MFMarcos Flores-Alamo
Marcos Flores-Alamo
JGJuventino J. García
Juventino J. García

5 September 2022 in Inorganics
Verified
Journal Article
Open access
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Alberto Aragón-MurielAlberto Aragón-Muriel
Alberto Aragón-Muriel
VIVIANA REYES MARQUEZVIVIANA REYES MARQUEZ
VIVIANA REYES MARQUEZ
FCFarrah Cañavera-Buelvas
Farrah Cañavera-Buelvas
JUJesus Ricardo Parra Unda
Jesus Ricardo Parra Unda
Fernando Cuenú-CabezasFernando Cuenú-Cabezas
Fernando Cuenú-Cabezas
DAVID MORALES-MORALESDAVID MORALES-MORALES
DAVID MORALES-MORALES
Within the current challenges in medicinal chemistry, the development of new and better therapeutic agents effective against infectious diseases produced by bacteria, fungi, viruses, and parasites stands out. With chemotherapy as one of the main strategies against these diseases focusing on the administration of organic and inorganic drugs, the latter is generally based on the synergistic effect produced by the formation of metal complexes with biologically active organic compounds. In this sense, Schiff bases (SBs) represent and ideal ligand scaffold since they have demonstrated a broad spectrum of antitumor, antiviral, antimicrobial, and anti-inflammatory activities, among others. In addition, SBs are synthesized in an easy manner from one-step condensation reactions, being thus suitable for facile structural modifications, having the imine group as a coordination point found in most of their metal complexes, and promoting chelation when other donor atoms are three, four, or five bonds apart. However, despite the wide variety of metal complexes found in the literature using this type of ligands, only a handful of them include on their structures tridentate SBs ligands and their biological evaluation has been explored. Hence, this review summarizes the most important antimicrobial activity results reported this far for pincer-type complexes (main group and d-block) derived from SBs tridentate ligands.

15 May 2009 in Journal of Organometallic Chemistry
Verified
Journal Article
Closed access
AAAlejandro J. Arce
Alejandro J. Arce
FCFarrah Cañavera-Buelvas
Farrah Cañavera-Buelvas
YSYsaura De Sanctis
Ysaura De Sanctis
JAJulian Ascanio
Julian Ascanio
RMRubén Machado
Rubén Machado
TGTeresa González
Teresa González

1 June 2004 in Journal of Organometallic Chemistry
Verified
Journal Article
Closed access
YSYsaura De Sanctis
Ysaura De Sanctis
AAAlejandro J. Arce
Alejandro J. Arce
FCFarrah Cañavera-Buelvas
Farrah Cañavera-Buelvas
RMRuben Machado
Ruben Machado
ADAntony J. Deeming
Antony J. Deeming
EGEsperanza Galarza
Esperanza Galarza


26 March 2011 in Acta Crystallographica Section E Structure Reports Online
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Journal Article
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FCFarrah Cañavera-Buelvas
Farrah Cañavera-Buelvas
MFMarcos Flores-Alamo
Marcos Flores-Alamo
JGJuventino J. García
Juventino J. García
In the title compound, [NiCl(2)(C(14)H(32)P(2))]·2C(12)H(9)N, the neutral [Ni(dppe)Cl(2)] complex [dppe is 1,2-bis-(diisopropyl-phosphan-yl)ethane] consists of a tetracoordinated Ni(2+) cation and has a crystallographic twofold axis passing through the metal atom and the mid-point of the CH(2)-CH(2) bond of the dppe ligand. The metal atom shows slight tetra-hedral distortion from an ideal square-planar coordination geometry, as reflected in the dihedral angle between NiCl(2) and NiP(2) planes of 15.32 (2)°. The 9H-carbazole ring system is essentially planar (r.m.s. deviation = 0.022 Å). In the crystal packing, there are two symmetry-related 9H-carbazole mol-ecules between two adjacent Ni(II) complexes, with an angle between the carbazole mean planes of ca 77°.