Daniel Łowicki

ORCID: 0000-0002-0405-5565
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About
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Research Areas
  • Coccidia and coccidiosis research
  • Veterinary medicine and infectious diseases
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Asymmetric Hydrogenation and Catalysis
  • Asymmetric Synthesis and Catalysis
  • Antibiotics Pharmacokinetics and Efficacy
  • Glycosylation and Glycoproteins Research
  • Surface Chemistry and Catalysis
  • Pesticide Residue Analysis and Safety
  • Insect and Pesticide Research
  • Nuclear Materials and Properties
  • Chemical Synthesis and Analysis
  • Diet, Metabolism, and Disease
  • Synthesis and Catalytic Reactions
  • Analytical Chemistry and Sensors
  • Organoboron and organosilicon chemistry
  • Synthetic Organic Chemistry Methods
  • Analytical Methods in Pharmaceuticals
  • Carbon dioxide utilization in catalysis
  • Organometallic Complex Synthesis and Catalysis
  • Diphtheria, Corynebacterium, and Tetanus
  • Analytical Chemistry and Chromatography
  • Carbohydrate Chemistry and Synthesis
  • Chemical Thermodynamics and Molecular Structure

Adam Mickiewicz University in Poznań
2007-2022

Jagiellonian University
2013-2015

10.1016/j.bbamem.2012.04.017 article EN publisher-specific-oa Biochimica et Biophysica Acta (BBA) - Biomembranes 2012-05-01

Abstract A highly efficient asymmetric hydrosilylation (AHS) of a wide variety prochiral aryl ketones catalyzed by zinc acetate with TPS‐he‐pybox ( tert ‐butyldiphenylsilyl hydroxyethyl pybox) ligand has been successfully developed. Cheap and readily available chiral Lewis acids based on salts have used as promising catalyst for the reduction under mild conditions at room temperature leading to alcohols in excellent yields good high enantioselectivities (up 85% ee ). magnified image

10.1002/adsc.201300682 article EN Advanced Synthesis & Catalysis 2014-02-06
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