Eduardo Pena-Cabrera
Overview
Explore the profile of Eduardo Pena-Cabrera including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
42
Citations
284
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Oliden-Sanchez A, Alvarado-Martinez E, Ramirez-Ornelas D, Vazquez M, Avellanal-Zaballa E, Banuelos J, et al.
Molecules
. 2023 Jun;
28(12).
PMID: 37375305
Herein, we report the synthetic access to a set of π-extended BODIPYs featuring a penta-arylated (phenyl and/or thiophene) dipyrrin framework. We take advantage of the full chemoselective control of 8-methylthio-2,3,5,6-tetrabromoBODIPY...
2.
Velazco-Cabral I, Vazquez J, Alcaraz-Contreras Y, Delgado F, Pena-Cabrera E, Garcia Revilla M, et al.
J Org Chem
. 2023 Jun;
88(14):9615-9628.
PMID: 37307088
A novel synthetic methodology is reported for the synthesis of fluorescent pyrrolo[1,2-]pyrimidines. Fischer carbene complexes served as the synthetic platform for (3+3) cyclization to form the heterocyclic moiety. The reaction...
3.
Arroyo-Cordoba I, Gamboa-Velazquez G, Avila-Ortiz C, Leyva-Ramirez M, Cortez-Picasso M, Garcia-Revilla M, et al.
ChemistryOpen
. 2022 Oct;
11(10):e202200197.
PMID: 36284210
Two novel BODIPY-Ugi (boron dipyrromethene) adducts exhibit peculiar room temperature (T=20 °C) H-1 NMR spectra in that several protons located at the aromatic aniline-type ring are lost in the baseline....
4.
Vazquez J, Velazco-Cabral I, Flores-Alamo M, Turlakov G, Rodriguez G, Moggio I, et al.
Chemistry
. 2022 Sep;
28(71):e202202446.
PMID: 36123302
A series of new symmetrical highly substituted BODIPYs 6 a-l was synthesized through a prefunctionalization approach in 35 %-89 % yields from the pyrrole core. This strategy allowed modulation of...
5.
Vazquez J, Velazco-Cabral I, Alvarado-Mendez E, Trejo-Duran M, Flores-Alamo M, Pena-Cabrera E, et al.
Phys Chem Chem Phys
. 2021 Sep;
23(39):22466-22475.
PMID: 34585696
A series of new coumarin-imidazo[1,2-]heterocyclic-3-acrylate derivatives 7a-h were synthesized by the Heck reaction between the corresponding 3-(imidazo[1,2-]pyrimidines)-(2-yl)-2-chromen-2-ones 4a-e and methyl acrylate in 45-87% yields. The effect of the distinct substituents...
6.
Reviriego F, Pena-Cabrera E, Kokate S, Alkorta I, Elguero J
Magn Reson Chem
. 2020 Nov;
59(4):454-464.
PMID: 33217045
10-Hydrazino-BODIPY, BoNHNH , presents slow rotation about the C10-NH bond that results in anisochronous H and C NMR signals. The assignment of the different signals has been made using traditional...
7.
Mitkari S, Medina-Ortiz A, Olivares-Romero J, Vazquez M, Pena-Cabrera E, Villegas Gomez C, et al.
Chemistry
. 2020 Nov;
27(2):618-621.
PMID: 33169452
An aminocatalytic privileged diversity-oriented synthesis (ApDOS) strategy utilizing trienamine catalysis for the construction of diverse and complex thiopyrans-piperidone fused rings through a thia-Diels-Alder/nucleophilic ring-closing sequence by using dithioamides as activated...
8.
Staniszewska M, Sobiepanek A, Gizinska M, Pena-Cabrera E, Arroyo-Cordoba I, Kazek M, et al.
Eur J Med Chem
. 2020 Feb;
191:112139.
PMID: 32109777
Since our study showed that sulfone derivatives' action mode creates a lesser risk of inducing widespread resistance among Candida spp., we continued verifying sulfones' antifungal activity using the following newly...
9.
Enriquez-Palacios E, Arbeloa T, Banuelos J, Bautista-Hernandez C, Becerra-Gonzalez J, Lopez-Arbeloa I, et al.
Molecules
. 2020 Feb;
25(4).
PMID: 32059435
Herein we report on a straightforward access method for boron dipyrromethene dyes (BODIPYs)-coumarin hybrids linked through their respective 8- and 6- positions, with wide functionalization of the coumarin fragment, using...
10.
Guerrero-Corella A, Asenjo-Pascual J, Pawar T, Diaz-Tendero S, Martin-Somer A, Villegas Gomez C, et al.
Chem Sci
. 2019 May;
10(15):4346-4351.
PMID: 31057762
In this work we have found that a BODIPY can be used as an electron withdrawing group for the activation of double bonds in asymmetric catalysis. The synthesis of cyclohexyl...