Radomir Jasiński - Concepedia

Author

Radomir Jasiński

Also Known As

Jasinski, Radomir, Jasiński, Radomir, R. Jasinski, R. Jasiński, Radomir A. Jasiński, Radomir JASIŃSKI, Radomir Jasinski, Radomir Jasiski, Radomir JasiÅski, Radomir Jasiński

242

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Cracow University of Technology Institute of Organic Chemistry Maria Curie-Skłodowska University Łukasiewicz Research Network - Institute of Heavy Organic Synthesis "Blachownia"

About

Radomir Jasiński is an author at Cracow University of Technology specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	24	52	1.5K
2	Natural Sciences	19	33	855
3	Biochemistry	15	17	391
4	Applied Physics	2	2	75
5	Medicine	1	1	40

Radomir Jasiński

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
A stepwise, zwitterionic mechanism for the 1,3-dipolar cycloaddition between (Z)-C-4-methoxyphenyl-N-phenylnitrone and gem-chloronitroethene catalysed by 1-butyl-3-methylimidazolium ionic liquid cations Radomir Jasiński Tetrahedron Letters Chemical EngineeringNovel OrganocatalystsEngineeringHeterocyclic1,3-Dipolar Cycloaddition	2014	125
Green in water sonochemical synthesis of tetrazolopyrimidine derivatives by a novel core-shell magnetic nanostructure catalyst Ali Maleki, Jamal Rahimi, Oleg M. Demchuk, Ultrasonics Sonochemistry	2017	102
Searching for zwitterionic intermediates in Hetero Diels–Alder reactions between methyl α,p-dinitrocinnamate and vinyl-alkyl ethers Radomir Jasiński Computational and Theoretical Chemistry Chemical EngineeringEngineeringAlkene MetathesisOrganic ChemistryHetero Diels–alder Reactions	2014	75
An experimental and theoretical study of the hetero Diels–Alder reactions between (E)-2-aryl-1-cyano-1-nitroethenes and ethyl vinyl ether: one-step or zwitterionic, two-step mechanism? Radomir Jasiński, M. Kubik, Agnieszka Łapczuk-Krygier, Reaction Kinetics Mechanisms and Catalysis	2014	64
In the searching for zwitterionic intermediates on reaction paths of [3 + 2] cycloaddition reactions between 2,2,4,4-tetramethyl-3-thiocyclobutanone S-methylide and polymerizable olefins Radomir Jasiński RSC Advances 2,2,4,4-Tetramethyl-3-thiocyclobutanone S-methylideEngineeringHeterocyclicAlkene MetathesisNatural Sciences	2015	62
Competition between the one-step and two-step, zwitterionic mechanisms in the [2+3] cycloaddition of gem-dinitroethene with (Z)-C,N-diphenylnitrone: a DFT computational study Radomir Jasiński Tetrahedron EngineeringHeterocyclicPhysicsNatural SciencesApplied Physics	2012	60
Regio- and stereoselectivity of polar [2+3] cycloaddition reactions between (Z)-C-(3,4,5-trimethoxyphenyl)-N-methylnitrone and selected (E)-2-substituted nitroethenes Radomir Jasiński, Magda Ziółkowska, Agata Maziarka Open Chemistry Yield MixturesChemical EngineeringEngineeringHeterocyclicAlkene Metathesis	2014	59
A DFT computational study of the molecular mechanism of [3 + 2] cycloaddition reactions between nitroethene and benzonitrile N-oxides Radomir Jasiński, Ewa Jasińska, Ewa Dresler Journal of Molecular Modeling	2016	56
β-Trifluoromethylated nitroethenes in Diels-Alder reaction with cyclopentadiene: A DFT computational study Radomir Jasiński Journal of Fluorine Chemistry Chemical Engineeringβ-Trifluoromethylated NitroethenesEngineeringAlkene MetathesisOrganic Chemistry	2017	53
A reexamination of the molecular mechanism of the Diels–Alder reaction between tetrafluoroethene and cyclopentadiene Radomir Jasiński Reaction Kinetics Mechanisms and Catalysis Organic Charge-transfer CompoundEngineeringHeterocyclicAlkene MetathesisNatural Sciences	2016	52

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