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Chemistry

D-Index
40
Citations
5496
World Ranking
17915
National Ranking
13

Overview

Stojan Stavber is affiliated with the Jožef Stefan Institute in Slovenia and specializes in the field of Chemistry, with a strong focus on Organic Chemistry and related subfields. Their research encompasses various aspects of chemical synthesis, catalytic reactions, and corrosion behavior.

The scientist's main fields of study include:

  • Chemistry

Within this broad domain, they concentrate on several subfields:

  • Organic Chemistry
  • Inorganic Chemistry
  • Molecular Biology
  • Materials Chemistry
  • Civil and Structural Engineering

Their research topics cover a spectrum of areas relevant to synthesis and catalysis, corrosion science, and molecular interactions:

  • Chemical Synthesis and Reactions
  • Synthesis and Catalytic Reactions
  • Catalytic C-H Functionalization Methods
  • Corrosion Behavior and Inhibition
  • Concrete Corrosion and Durability
  • Asymmetric Hydrogenation and Catalysis
  • Crystallography and Molecular Interactions

Stavber has contributed to several peer-reviewed articles in scientific journals, including:

  • "Simplistic correlations between molecular electronic properties and inhibition efficiencies: Do they really exist?", 2020, Corrosion Science
  • "Editors' Choice-The Effect of Anchor Group and Alkyl Backbone Chain on Performance of Organic Compounds as Corrosion Inhibitors for Aluminum Investigated Using an Integrative Experimental-Modeling Approach", 2020, Journal of The Electrochemical Society
  • "Electrophilic Iodination of Organic Compounds Using Elemental Iodine or Iodides: Recent Advances 2008-2021: Part I", 2022, Compounds
  • "N-Halosuccinimides as Precatalysts for C-, N-, O-, and X-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions", 2020, Catalysts
  • "N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions", 2020, Catalysts

Their publications have appeared in multiple venues, with the most frequent being:

  • Catalysts (5 publications)
  • Corrosion Science
  • Journal of The Electrochemical Society
  • Compounds
  • Tetrahedron Letters

Collaboration is a notable component of Stavber's research, with frequent co-authors including:

  • Njomza Ajvazi
  • Anton Kokalj
  • Ingrid Milošev
  • Bojan Božić
  • Matic Lozinšek

Best Publications

  • Electrophilic Iodination of Organic Compounds Using Elemental Iodine or Iodides

    Stojan Stavber;Marjan Jereb;Marko Zupan

  • Bromination of ketones with H2O2–HBr “on water”

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Marko Zupan;Jernej Iskra

  • Halogenation of ketones with N-halosuccinimides under solvent-free reaction conditions

    Igor Pravst;Marko Zupan;Marko Zupan;Stojan Stavber

  • Environmentally benign electrophilic and radical bromination 'on water': H2O2-HBr system versus N-bromosuccinimide

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Jernej Iskra

  • Simplistic correlations between molecular electronic properties and inhibition efficiencies: Do they really exist?

    Anton Kokalj;Matic Lozinšek;Barbara Kapun;Peyman Taheri

  • Iodine as a catalyst for efficient conversion of ketones to gem-dihydroperoxides by aqueous hydrogen peroxide.

    Katja Zmitek;Marko Zupan;Stojan Stavber;Jernej Iskra

  • The effect of iodine on the peroxidation of carbonyl compounds.

    Katja Zmitek;Marko Zupan;Stojan Stavber;Jernej Iskra

  • Halogenation of organic compounds in ionic liquids

    Jasminka Pavlinac;Marko Zupan;Kenneth K. Laali;Stojan Stavber

  • Selective and effective fluorination of organic compounds in water using Selectfluor F-TEDA-BF4.

    Gaj Stavber;Marko Zupan;Marjan Jereb;Stojan Stavber

  • Visible light induced ‘on water’ benzylic bromination with N-bromosuccinimide

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Jernej Iskra

  • Recent Advances in the Application of SelectfluorTMF-TEDA-BF4 as a Versatile Mediator or Catalyst in Organic Synthesis

    Stojan Stavber

  • Directed regioselectivity of bromination of ketones with NBS: solvent-free conditions versus water

    Igor Pravst;Marko Zupan;Marko Zupan;Stojan Stavber

  • Selective aerobic oxidative dibromination of alkenes with aqueous HBr and sodium nitrite as a catalyst

    Ajda Podgoršek;Marco Eissen;Jens Fleckenstein;Stojan Stavber

  • Free radical bromination by the H2O2–HBr system on water

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Marko Zupan;Jernej Iskra

  • Fluorination with cesium fluoroxysulfate. Room-temperature fluorination of benzene and naphthalene derivatives

    Stojan Stavber;Marko Zupan

  • Nonmetal-Catalyzed Iodination of Arenes with Iodide and Hydrogen Peroxide

    Jernej Iskra;Stojan Stavber;Marko Zupan

  • Solvent-free bromination of 1,3-diketones and β-keto esters with NBS

    Igor Pravst;Marko Zupan;Marko Zupan;Stojan Stavber

  • High yield direct fluorofunctionalisation of ketones using AccufluorTM-NFTh fluorinating reagent

    Stojan Stavber;Marko Zupan

  • Ritter-type fluorofunctionalisation as a new, effective method for conversion of alkenes to vicinal fluoroamides

    Stojan Stavber;Tjasa Sotler Pecan;Maja Papež;Marko Zupan

  • Micellar-System-Mediated DirectFluorination of Ketones in Water

    Gaj Stavber;Marko Zupan;Stojan Stavber

Frequent Co-Authors

Ingrid Milošev
Ingrid Milošev Jožef Stefan Institute
Anton Kokalj
Anton Kokalj Jožef Stefan Institute
Boris Sket
Boris Sket University of Ljubljana
John A. Gladysz
John A. Gladysz Texas A&M University
Jean'ne M. Shreeve
Jean'ne M. Shreeve University of Idaho
Barbara Malič
Barbara Malič Jožef Stefan Institute
Kaoru Nakamura
Kaoru Nakamura Kobe University
Atta-ur-Rahman
Atta-ur-Rahman University of Karachi
Marija Kosec
Marija Kosec Jožef Stefan Institute
G. K. Surya Prakash
G. K. Surya Prakash University of Southern California

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