Denisse de Loera

ORCID: 0000-0002-5291-2197
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About
Contact & Profiles
Research Areas
  • Synthesis and Biological Evaluation
  • Chemical Reactions and Mechanisms
  • Bioactive Compounds and Antitumor Agents
  • Synthesis and biological activity
  • Multicomponent Synthesis of Heterocycles
  • Synthesis and Catalytic Reactions
  • Chemistry and Chemical Engineering
  • Cancer therapeutics and mechanisms
  • Chemical Reaction Mechanisms
  • Phytochemistry and Biological Activities
  • Chemical Synthesis and Analysis
  • Morinda citrifolia extract uses
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Garlic and Onion Studies
  • Click Chemistry and Applications
  • Organic Chemistry Cycloaddition Reactions
  • Mesoporous Materials and Catalysis
  • Pharmacological Effects of Natural Compounds
  • Toxin Mechanisms and Immunotoxins
  • Plant-derived Lignans Synthesis and Bioactivity
  • Essential Oils and Antimicrobial Activity
  • Sulfur-Based Synthesis Techniques
  • Radical Photochemical Reactions
  • Synthesis of Tetrazole Derivatives
  • Synthesis of β-Lactam Compounds

Autonomous University of San Luis Potosí
2014-2025

Université Laval
2022

Institute for Biomedical and Pharmaceutical Research
2022

University of Bonn
2022

The University of Texas MD Anderson Cancer Center
2022

UCLouvain
2022

University of California, Los Angeles
2012-2013

The photoinduced and thermal denitrogenation of crystalline triazolines with bulky substituents leads to the quantitative formation aziridines in clean solid-to-solid reactions despite very large structural changes transition from reactant product. Analysis reaction progress by powder X-ray diffraction, solid-state (13)C CPMAS NMR, FTIR spectroscopy, analysis has revealed that proceed either through metastable phases susceptible amorphization or mechanisms involve a reconstructive phase...

10.1021/ja401577p article EN Journal of the American Chemical Society 2013-04-02

A new synthetic strategy to obtain linked 1,5-disubstituted tetrazole-1,2,3-triazoles via the Ugi-azide reaction followed by a copper-catalyzed alkyne-azide (CuAAC) was developed. This used solvent-free conditions for reaction. two-step affords products in moderate good yields. To best of our knowledge, this is first report using CuAAC as post-condensation process an and therefore, describing synthesis tetrazole (1,5-DS-T) 1,2,3-triazole moiety, which are molecules that may have potential...

10.1080/00397911.2019.1616301 article EN Synthetic Communications 2019-05-20

The solid-state photodenitrogenation of crystalline triazolines proceeds with high efficiency to form the corresponding aziridines in chemical yields upon selection proper irradiation wavelength. It was shown that solid-to-solid reactions occur by formation product metastable phases.

10.1021/ol301582n article EN Organic Letters 2012-07-13

We performed an extensive analysis about the reaction conditions of 1,4-Michael addition amino acids to 1,4-naphthoquinone and substitution 2,3-dichloronaphthoquinone, a complete evaluation stoichiometry, use different bases, pH influence was performed. were able show that microwave-assisted synthesis is best method for naphthoquinone–amino acid chloride–naphthoquinone–amino derivatives with 79–91% 78–91% yields, respectively. The cyclic voltammetry profiles showed both series mainly display...

10.3390/molecules24234285 article EN cc-by Molecules 2019-11-25

We previously showed that microwave assisted synthesis is the best method for of naphthoquinone amino acid and chloride-naphthoquinone derivatives by a complete evaluation reaction conditions such as stoichiometry, bases, pH influence. Following same strategy, we synthesized chloride non-chloride tyrosine, valine, tryptophan-naphthoquinones achieving 85–95%, 80–92%, 91–95% yields, respectively. The cyclic voltammetry profiles both series mainly display one redox process. Overall, exhibited...

10.3390/molecules25092058 article EN cc-by Molecules 2020-04-28

Snow mountain garlic is traditionally eaten by Himalayan locals for its medicinal properties. Although different species of the genus

10.3390/molecules29204958 article EN cc-by Molecules 2024-10-20

<b><i>Background:</i></b> Fluoroquinolones are widely prescribed synthetic antimicrobial agents. Quinolones act by converting their targets, gyrase and topoisomerase IV, into toxic enzymes that fragment the bacterial chromosome; irreversible DNA damage eventually causes killing of bacteria. Thorough knowledge structure-activity relationship quinolones is essential for development new drugs with improved activity against resistant strains....

10.1159/000456533 article EN Chemotherapy 2017-01-01

Mannich bases are formed in a noncatalytic multicomponent reaction, which is promoted by ultrasound irradiation. The procedure avoids the use of toxic solvents, catalyst, and purification, generating desired compounds excellent yields short reaction times.

10.1080/00397911.2017.1371760 article EN Synthetic Communications 2017-09-07

Heterogeneous photocatalysis is widely used in a broad variety of chemical reactions such as oxidations, dehydrogenation and hydrogen transfer. The photocatalyzed reduction nitro groups has been to prepare organic compounds with important industrial biological applications. formation the desired compound could be controlled by selecting adequate reaction conditions catalyst solvent. This review presents overview mechanisms photocatalytic nitrobenzene develop viable route produce sole or...

10.2174/1385272822666180704144904 article EN Current Organic Chemistry 2018-07-05

The hydantoin moiety is found in several bioactive compounds with important pharmacological properties such as antimicrobial, antifungal, anti-androgens, anticancer and the historical action anticonvulsant. Because of these reasons, synthesis their derivatives to review considering philosophy green chemistry. In this review, we present actual importance hydantoins using methods, microwave ultrasound irradiation, ionic liquids, solid-phase solvent-free synthesis. Finally, protocols reported...

10.2174/1570193x16666181206100225 article EN Mini-Reviews in Organic Chemistry 2018-12-07

The nitrogen inversion of a N-phenyl aziridine fused to succinimide ring is influenced by the presence phenyl in moiety. endo invertomer favored, showing an unsymmetrical equilibrium variable (1)H NMR studies.

10.1021/jo4022315 article EN The Journal of Organic Chemistry 2013-10-14

1,4-naftoquinone (NQ) molecules have been extensively evaluated as potent antibacterial compounds; however, their use is limited, since they low water solubility and exhibit toxicities in healthy eukaryotic cells. A possible path to overcoming these challenges the of particulate vehicles, such SBA-15, which a biocompatible biodegradable mesoporous silica material, that may enhance drug delivery decrease dosages. In this work, an isotherm model-based adsorption three NQs into SBA-15...

10.3390/ph15121464 article EN cc-by Pharmaceuticals 2022-11-25

The synthesis and biological evaluation of 1,4-naphthoquinone derivatives are great interest since these compounds exhibit strong antibacterial, antifungal, antimalarial, anticancer activities. electronic properties naphthoquinones usually modulated by attaching functional groups containing nitrogen, oxygen sulfur atoms, which tune their potency selectivity.A series 13 amino acid were synthesized under assisted microwave ultrasound conditions. antibacterial activity was tested against...

10.1159/000521098 article EN Chemotherapy 2021-11-26
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