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D-Index & Metrics

Chemistry

D-Index
52
Citations
10975
World Ranking
13431
National Ranking
13

Research.com Recognitions

  • 2009 - Fellow of the American Chemical Society

Overview

Eusebio Juaristi is affiliated with the Instituto Politécnico Nacional in Mexico and has a research focus primarily in the fields of Chemistry and Materials Science. Their scientific contributions span several interdisciplinary areas, with a significant focus on Organic Chemistry and Materials Chemistry. Additional subfields of study include Molecular Biology, Physical and Theoretical Chemistry, and Pharmacology.

Juaristi's research topics encompass a range of themes related to chemical synthesis and analysis, asymmetric synthesis and catalysis, and crystallographic methods. Specific areas of expertise include:

  • Chemical Synthesis and Analysis
  • Asymmetric Synthesis and Catalysis
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Chemical Synthesis and Reactions
  • Computational Drug Discovery Methods
  • Crystallography and Molecular Interactions

Their recent publications illustrate ongoing contributions to advancing mechanochemical methods and sustainable organic synthesis. Selected papers include:

  • "Mechanochemical and Mechanoenzymatic Synthesis of Pharmacologically Active Compounds: A Green Perspective," 2020, ACS Sustainable Chemistry & Engineering
  • "Salient Achievements in Synthetic Organic Chemistry Enabled by Mechanochemical Activation," 2023, Synthesis
  • "Recent Developments in Next Generation (S)-Proline-Derived Chiral Organocatalysts," 2021, Tetrahedron
  • "Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions," 2020, Molecules
  • "Mechanoenzymology: State of the Art and Challenges towards Highly Sustainable Biocatalysis," 2021, ChemSusChem

Frequent collaborators in their research include Jaime Escalante, C.G. Ávila-Ortíz, Jonathan Román Valdéz-Camacho, Mario Pérez-Venegas, and Adrián Espinoza-Guillén. These partnerships highlight multidisciplinary teamwork within their specialization.

Publication venues where Juaristi's work frequently appears include The Cambridge Structural Database, European Journal of Organic Chemistry, Molecules, Synthesis, and Tetrahedron. This range demonstrates a presence in journals focused on structural databases, organic chemistry, and molecular sciences.

In addition to journal articles, they have contributed to book publications, including a volume titled "Technology, Science and Culture - A Global Vision, Volume IV" published by IntechOpen in 2023.

Juaristi's career has been recognized by awards such as the Fellow of the American Chemical Society in 2009, indicating acknowledgement by a major professional organization within the chemistry community.

Best Publications

  • Recent studies of the anomeric effect

    Eusebio Juaristi;Gabriel Cuevas

  • Recent advances in the enantioselective synthesis of beta-amino acids.

    E Juaristi;H López-Ruiz

  • The anomeric effect

    Eusebio Juaristi;Gabriel Cuevas

  • Addition of chiral glycine, methionine, and vinylglycine enolate derivatives to aldehydes and ketones in the preparation of enantiomerically pure α-amino-β-hydroxy acids

    Dieter Seebach;Eusebio Juaristi;David D. Miller;Christof Schickli

  • Recent efforts directed to the development of more sustainable asymmetric organocatalysis

    José G. Hernández;Eusebio Juaristi

  • Introduction to Stereochemistry and Conformational Analysis

    Eusebio Juaristi

  • Asymmetric aldol reaction organocatalyzed by (S)-proline-containing dipeptides: improved stereoinduction under solvent-free conditions.

    José G. Hernández;Eusebio Juaristi

  • Mechanochemical and Mechanoenzymatic Synthesis of Pharmacologically Active Compounds: A Green Perspective

    Mario Pérez-Venegas;Eusebio Juaristi

  • Recent applications of α-phenylethylamine (α-PEA) in the preparation of enantiopure compounds. Part 3: α-PEA as chiral auxiliary. Part 4: α-PEA as chiral reagent in the stereodifferentiation of prochiral substrates

    Eusebio Juaristi;José Luis León-Romo;Adelfo Reyes;Jaime Escalante

  • Solvent-free asymmetric aldol reaction organocatalyzed by (S)-proline-containing thiodipeptides under ball-milling conditions

    José G. Hernández;Víctor García-López;Eusebio Juaristi

  • Enantioselective Aldol and Michael Additions of Achiral Enolates in the Presence of Chiral Lithium Amides and Amines

    Eusebio Juaristi;Albert K. Beck;Jesper Hansen;Thomas Matt

  • Structure and Reactivity of Five- and Six-Ring N, N-, N, O-, and O, O-acetals: A lesson in allylic 1, 3-strain (A1, 3 strain)

    Dieter Seebach;Bernd Amatsch;René Amstutz;Albert K. Beck

  • Green synthesis of α,β- and β,β-dipeptides under solvent-free conditions.

    José G. Hernández;Eusebio Juaristi

  • Recent applications of α-phenylethylamine (α-PEA) in the preparation of enantiopure compounds. Part 1: Incorporation in chiral catalysts. Part 2: α-PEA and derivatives as resolving agents

    Eusebio Juaristi;Jaime Escalante;José Luis León-Romo;Adelfo Reyes

  • Manifestation of Stereoelectronic Effects on the Calculated Carbon−Hydrogen Bond Lengths and One Bond 1JC-H NMR Coupling Constants in Cyclohexane, Six-Membered Heterocycles, and Cyclohexanone Derivatives

    Gabriel Cuevas;Eusebio Juaristi

  • The attractive and repulsive gauche effects

    Eusebio Juaristi

  • Stereoelectronic Interpretation for the Anomalous 1H NMR Chemical Shifts and One-Bond C-H Coupling Constants (Perlin Effects) in 1,3-Dioxanes, 1,3-Oxathianes, and 1,3-Dithianes. Spectroscopic and Theoretical Observations

    Eusebio Juaristi;Gabriel Cuevas;Alberto Vela

  • Use of diamines containing the α-phenylethyl group as chiral ligands in the asymmetric hydrosilylation of prochiral ketones

    Virginia M. Mastranzo;Virginia M. Mastranzo;Leticia Quintero;Cecilia Anaya de Parrodi;Eusebio Juaristi

  • Efficient ball-mill procedure in the ‘green’ asymmetric aldol reaction organocatalyzed by (S)-proline-containing dipeptides in the presence of water

    José G. Hernández;Eusebio Juaristi

  • Asymmetric synthesis of .beta.-amino acids. 1. Highly diastereoselective addition of a racemic .beta.-alanine enolate derivative to electrophiles

    Eusebio Juaristi;Delia Quintana;Bernd Lamatsch;Dieter Seebach

  • Recent Advances in the Enantioselective Synthesis of β-Amino Acids

    Eusebio Juaristi;Heraclio Lopez‐Ruiz

Frequent Co-Authors

Dieter Seebach
Dieter Seebach ETH Zurich
Richard S. Glass
Richard S. Glass University of Arizona
Patrick J. Walsh
Patrick J. Walsh University of Pennsylvania
Akhilesh K. Verma
Akhilesh K. Verma University of Delhi
Ronald J. Nachman
Ronald J. Nachman United States Department of Agriculture
Ernest L. Eliel
Ernest L. Eliel University of Notre Dame
Alberto Vela
Alberto Vela CINVESTAV
George D. Wilson
George D. Wilson Beaumont Health
Elies Molins
Elies Molins Institut de Ciència de Materials de Barcelona
Andrew T. McPhail
Andrew T. McPhail Duke University

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