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D-Index
94
Citations
26803
World Ranking
1735
National Ranking
34

Overview

Vadim A. Soloshonok is affiliated with the University of the Basque Country in Spain. Their research primarily focuses on the field of Chemistry, with a significant emphasis on Organic Chemistry, Molecular Biology, Pharmaceutical Science, Inorganic Chemistry, and Materials Chemistry.

Their work covers a broad range of topics, including:

  • Chemical Synthesis and Analysis
  • Fluorine in Organic Chemistry
  • Click Chemistry and Applications
  • Asymmetric Hydrogenation and Catalysis
  • Asymmetric Synthesis and Catalysis
  • Carbohydrate Chemistry and Synthesis
  • Cyclopropane Reaction Mechanisms

Vadim A. Soloshonok has published extensively in various scientific venues. Frequent publication venues include:

  • Chinese Chemical Letters
  • Chemistry - A European Journal
  • Chirality
  • The Cambridge Structural Database
  • Journal of Fluorine Chemistry

Among recent papers authored are:

  • Next generation organofluorine containing blockbuster drugs, 2020, Journal of Fluorine Chemistry
  • Fluorine-containing drugs approved by the FDA in 2019, 2020, Chinese Chemical Letters
  • Fluorine-containing pharmaceuticals approved by the FDA in 2020: Synthesis and biological activity, 2021, Chinese Chemical Letters
  • Fluorine-containing drugs approved by the FDA in 2021, 2022, Chinese Chemical Letters
  • Cyclic tailor-made amino acids in the design of modern pharmaceuticals, 2020, European Journal of Medicinal Chemistry

Vadim A. Soloshonok collaborates frequently with several researchers, including:

  • Jianlin Han
  • Hiroki Moriwaki
  • Hiroyuki Konno
  • Haibo Mei
  • Kunisuke Izawa

Best Publications

  • Fluorine in pharmaceutical industry: fluorine-containing drugs introduced to the market in the last decade (2001-2011).

    Jiang Wang;María Sánchez-Roselló;José Luis Aceña;Carlos del Pozo

  • Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II–III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas

    Yu Zhou;Jiang Wang;Zhanni Gu;Shuni Wang

  • Modern Approaches for Asymmetric Construction of Carbon–Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs

    Yi Zhu;Jianlin Han;Jiandong Wang;Norio Shibata

  • Recent advances in the trifluoromethylation methodology and new CF3-containing drugs

    Wei Zhu;Jiang Wang;Shuni Wang;Zhanni Gu

  • Fluorine-Containing Drugs Approved by the FDA in 2018

    Haibo Mei;Jianlin Han;Santos Fustero;Mercedes Medio‐Simon

  • Chemical Aspects of Human and Environmental Overload with Fluorine

    Jianlin Han;Loránd Kiss;Haibo Mei;Attila Márió Remete

  • Next generation organofluorine containing blockbuster drugs

    Jianlin Han;Attila Márió Remete;Luca S. Dobson;Lorand Kiss

  • Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome.

    Jianlin Han;Vadim A. Soloshonok;Vadim A. Soloshonok;Karel Douglas Klika;Józef Drabowicz

  • Fluorine-containing drugs approved by the FDA in 2019

    Haibo Mei;Attila Márió Remete;Yupiao Zou;Hiroki Moriwaki

  • Enantiocontrolled synthesis of fluoro-organic compounds : stereochemical challenges and biomedical targets

    V. A. Soloshonok

  • Remarkable Amplification of the Self‐Disproportionation of Enantiomers on Achiral‐Phase Chromatography Columns

    Vadim A. Soloshonok

  • Applications of fluorine-containing amino acids for drug design.

    Haibo Mei;Jianlin Han;Karel D. Klika;Kunisuke Izawa

  • Phenomenon of optical self-purification of chiral non-racemic compounds

    Vadim A. Soloshonok;Hisanori Ueki;Manabu Yasumoto;Shekar Mekala

  • Asymmetric synthesis of fluorine-containing amines, amino alcohols, α- and β-amino acids mediated by chiral sulfinyl group

    Alexander E. Sorochinsky;Vadim A. Soloshonok;Vadim A. Soloshonok

  • Fluorine-containing amino acids : synthesis and properties

    V. P. Kukharʹ;V. A. Soloshonok

  • Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 2: Aldol, Mannich addition reactions, deracemization and (S) to (R) interconversion of α-amino acids

    Alexander E. Sorochinsky;Alexander E. Sorochinsky;Alexander E. Sorochinsky;José Luis Aceña;Hiroki Moriwaki;Tatsunori Sato

  • Self-disproportionation of enantiomers via achiral chromatography: a warning and an extra dimension in optical purifications

    Vadim A. Soloshonok;Vadim A. Soloshonok;Christian Roussel;Osamu Kitagawa;Alexander E. Sorochinsky;Alexander E. Sorochinsky;Alexander E. Sorochinsky

  • Recent advances in the synthesis of fluorinated aminophosphonates and aminophosphonic acids

    Kostiantyn V. Turcheniuk;Valery P. Kukhar;Gerd-Volker Röschenthaler;José Luis Aceña

  • Fluorine-containing pharmaceuticals approved by the FDA in 2020: Synthesis and biological activity

    Yingjie Yu;Aiyao Liu;Gagan Dhawan;Haibo Mei

  • Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations

    Alexander E. Sorochinsky;José Luis Aceña;Hiroki Moriwaki;Tatsunori Sato

  • Asymmetric Synthesis of Phosphorus Analogs of Amino Acids

    V. P. Kukhar;V. A. Soloshonok;V. A. Solodenko

  • Recent Advances in the Asymmetric Synthesis of α-(Trifluoromethyl)-Containing α-Amino Acids

    José Luis Aceña;Alexander E. Sorochinsky;Alexander E. Sorochinsky;Alexander E. Sorochinsky;Vadim A. Soloshonok;Vadim A. Soloshonok

  • Rational application of self-disproportionation of enantiomers via sublimation—a novel methodological dimension for enantiomeric purifications

    Hisanori Ueki;Manabu Yasumoto;Vadim A. Soloshonok;Vadim A. Soloshonok

  • Asymmetric Catalysis of the Friedel−Crafts Reaction with Fluoral by Chiral Binaphthol-Derived Titanium Catalysts through Asymmetric Activation

    Akihiro Ishii;Vadim A. Soloshonok;Koichi Mikami

  • Erythro-Selective aldol-type reaction of N-sulfonylaldimines with methyl isocyanoacetate catalyzed by gold(I)

    Tamio Hayashi;Eiji Kishi;Vadim A. Soloshonok;Yasuhiro Uozumi

Frequent Co-Authors

Jianlin Han
Jianlin Han Nanjing Forestry University
Yi Pan
Yi Pan Nanjing University
Victor J. Hruby
Victor J. Hruby University of Arizona
Hong Liu
Hong Liu Shandong University
Santos Fustero
Santos Fustero University of Valencia
Norio Shibata
Norio Shibata Nagoya Institute of Technology
Yasufumi Ohfune
Yasufumi Ohfune Osaka Metropolitan University
Christian Roussel
Christian Roussel Aix-Marseille University
Tamio Hayashi
Tamio Hayashi National Taiwan Normal University

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