2003 - Fellow of John Simon Guggenheim Memorial Foundation
2000 - Fellow of Alfred P. Sloan Foundation
Thomas Lectka mostly deals with Catalysis, Organic chemistry, Enantioselective synthesis, Nucleophile and Combinatorial chemistry. His Catalysis research includes elements of Reactivity, Halogenation and Copper. His Medicinal chemistry research extends to the thematically linked field of Organic chemistry.
His Enantioselective synthesis research includes themes of Alkylation, Cycloaddition, Lewis acids and bases, Oxazoline and Stereochemistry. His Nucleophile research is multidisciplinary, relying on both Computational chemistry, Electrophile and Diphenylketene. His Combinatorial chemistry study combines topics in areas such as Isotopic labeling and Stoichiometry.
Thomas Lectka mainly focuses on Catalysis, Enantioselective synthesis, Organic chemistry, Combinatorial chemistry and Nucleophile. Thomas Lectka is interested in Lewis acids and bases, which is a field of Catalysis. His studies deal with areas such as Bifunctional, Amide and Imine as well as Lewis acids and bases.
The various areas that Thomas Lectka examines in his Enantioselective synthesis study include Amino acid, Alkylation, Cycloaddition and Oxazoline. Thomas Lectka works mostly in the field of Combinatorial chemistry, limiting it down to topics relating to Reactivity and, in certain cases, Molecule and Computational chemistry, as a part of the same area of interest. His Nucleophile research incorporates elements of Yield, Electrophile, Isomerization and Transition metal.
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Crystallography, Selectfluor and Molecule. His Catalysis study is related to the wider topic of Organic chemistry. His study in the field of Nucleophile, Enantioselective synthesis and Copper is also linked to topics like Beta-lactam and Chemical synthesis.
The study incorporates disciplines such as Reactivity, Halogenation and Regioselectivity in addition to Combinatorial chemistry. His Crystallography study integrates concerns from other disciplines, such as Nuclear magnetic resonance spectroscopy, Ring, Fluorine and Hydrogen bond. His biological study spans a wide range of topics, including Photochemistry, Electron paramagnetic resonance and Triethylborane.
Thomas Lectka focuses on Catalysis, Selectfluor, Organic chemistry, Molecule and Photochemistry. His Catalysis study combines topics from a wide range of disciplines, such as Combinatorial chemistry, Manganese and Photosensitizer. Thomas Lectka has researched Selectfluor in several fields, including Ketone, Triethylborane and Benzil.
His study in the field of Regioselectivity and Enantioselective synthesis also crosses realms of Beta-lactam and Chemical synthesis. His Molecule research is multidisciplinary, incorporating elements of Crystallography, Computational chemistry, Reactivity and Fluorine. His work in Photochemistry tackles topics such as Radical fluorination which are related to areas like Yield and Radical ion.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis
David J. Guerin;Scott J. Miller;Thomas Lectka.
Chemical Reviews (2003)
The Development of the First Catalyzed Reaction of Ketenes and Imines: Catalytic, Asymmetric Synthesis of β-Lactams
Andrew E. Taggi;Ahmed M. Hafez;Harald Wack;Brandon Young.
Journal of the American Chemical Society (2002)
CHIRAL BIS(OXAZOLINE)COPPER(II) COMPLEXES AS LEWIS ACID CATALYSTS FOR THE ENANTIOSELECTIVE DIELS-ALDER REACTION
David A. Evans;Scott J. Miller;Thomas Lectka;Peter von Matt.
Journal of the American Chemical Society (1999)
Bis(oxazoline)copper(II) complexes as chiral catalysts for the enantioselective Diels-Alder reaction
David A. Evans;Scott J. Miller;Thomas Lectka.
Journal of the American Chemical Society (1993)
Bifunctional Asymmetric Catalysis: Cooperative Lewis Acid/Base Systems
Daniel H. Paull;Ciby J. Abraham;Michael T. Scerba;Ethan Alden-Danforth.
Accounts of Chemical Research (2008)
Bis(oxazoline) and Bis(oxazolinyl)pyridine Copper Complexes as Enantioselective Diels−Alder Catalysts: Reaction Scope and Synthetic Applications
David A. Evans;David M. Barnes;Jeffrey S. Johnson;Thomas Lectka.
Journal of the American Chemical Society (1999)
Catalytic, Enantioselective Alkylation of α-Imino Esters Using Late Transition Metal Phosphine Complexes as Catalysts
Dana Ferraris;Brandon Young;Travis Dudding;Thomas Lectka.
Journal of the American Chemical Society (1998)
Catalytic, Asymmetric Synthesis of β-Lactams
Andrew E. Taggi;Ahmed M. Hafez;Harald Wack;Brandon Young.
Journal of the American Chemical Society (2000)
Alpha-imino esters: versatile substrates for the catalytic, asymmetric synthesis of alpha- and beta-amino acids and beta-lactams.
Andrew E. Taggi;and Ahmed M. Hafez;Thomas Lectka.
Accounts of Chemical Research (2003)
Chemical synthesis of β-lactams: asymmetric catalysis and other recent advances.
Cody Ross Pitts;Thomas Lectka.
Chemical Reviews (2014)
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