Michał Rachwalski - Concepedia

Author

Michał Rachwalski

University of Łódź ORCID

Also Known As

Micha.l Rachwalski, Michal Rachwalski, Michał Rachwalski

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of Łódź Polish Academy of Sciences Centrum Badań Molekularnych i Makromolekularnych Polskiej Akademii Nauk Radboud University Nijmegen Lodz University of Technology

About

Michał Rachwalski is an author at University of Łódź specializing in organic chemistry, engineering, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	19	33	739
2	Biomolecular Engineering	16	20	447
3	Natural Sciences	11	11	218
4	Chemical Engineering	10	10	244
5	Biochemistry	6	6	131

Michał Rachwalski

Publications

849

Citations

H-Index

Page 1

	Year	Citations
New highly efficient aziridine-functionalized tridentate sulfinyl catalysts for enantioselective diethylzinc addition to carbonyl compounds Stanisław Leśniak, Michał Rachwalski, Ewelina Sznajder, Tetrahedron Asymmetry Chemical EngineeringEngineeringOrganic ChemistryOrganometallic CatalysisCatalysis	2009	48
Highly enantioselective conjugate addition of diethylzinc to enones using aziridine-functionalized tridentate sulfinyl ligands Michał Rachwalski, Stanisław Leśniak, P. Kiełbasiński Tetrahedron Asymmetry EngineeringEnantioselective Conjugate AdditionOrganic ChemistryStereoselective SynthesisChemistry	2010	41
Lipase-promoted dynamic kinetic resolution of racemic β-hydroxyalkyl sulfones P. Kiełbasiński, Michał Rachwalski, M. Mikołajczyk, Tetrahedron Asymmetry BiochemistryNatural SciencesBiocatalysisBiochemical EngineeringRacemic β-Hydroxyalkyl Sulfones	2005	41
Enzyme-promoted desymmetrization of bis(2-hydroxymethylphenyl) sulfoxide as a route to tridentate chiral catalysts Michał Rachwalski, Małgorzata Kwiatkowska, J. Drabowicz, Tetrahedron Asymmetry EngineeringCatalytic SynthesisOrganic ChemistryEnzyme-promoted DesymmetrizationCatalysis	2008	37
Mandelic acid derived α-aziridinyl alcohols as highly efficient ligands for asymmetric additions of zinc organyls to aldehydes Michał Rachwalski, Szymon Jarzyński, Marcin Jasiński, Tetrahedron Asymmetry Efficient LigandsNovel OrganocatalystsEngineeringOrganic ChemistryOrganometallic Catalysis	2013	36
Highly enantioselective Henry reaction catalyzed by chiral tridentate heteroorganic ligands Michał Rachwalski, Stanisław Leśniak, Ewelina Sznajder, Tetrahedron Asymmetry Chemical EngineeringEngineeringOrganic ChemistryOrganometallic CatalysisCatalysis	2009	36
Aziridine ring-containing chiral ligands as highly efficient catalysts in asymmetric synthesis Michał Rachwalski, Szymon Jarzyński, Stanisław Leśniak Tetrahedron Asymmetry Chemical EngineeringEngineeringAsymmetric SynthesisOrganic ChemistryOrganometallic Catalysis	2013	32
Efficient catalysts for asymmetric Mannich reactions Michał Rachwalski, Tim Leenders, Sylwia Kaczmarczyk, Organic & Biomolecular Chemistry Cross-coupling ReactionEngineeringOrganic ChemistryMannich AdductsCatalysis	2013	32
Highly enantioselective addition of phenylethynylzinc to aldehydes using aziridine-functionalized tridentate sulfinyl ligands Michał Rachwalski, Stanisław Leśniak, P. Kiełbasiński Tetrahedron Asymmetry EngineeringOrganic ChemistryEnantioselective AdditionChemistryAsymmetric Catalysis	2010	31
N-Trityl-aziridinyl alcohols as highly efficient chiral catalysts in asymmetric additions of organozinc species to aldehydes Szymon Jarzyński, Stanisław Leśniak, Adam M. Pieczonka, Tetrahedron Asymmetry Asymmetric AdditionsEngineeringOrganic ChemistryOrganozinc SpeciesCatalysis	2014	28

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