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Martin Kotora

Martin Kotora

Charles University
Czech Republic

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

Organic chemistry, Catalysis, Medicinal chemistry, Enantioselective synthesis and Bipyridine are his primary areas of study. Martin Kotora carries out multidisciplinary research, doing studies in Organic chemistry and Metallocene. His studies deal with areas such as Aryl and Polymer chemistry as well as Catalysis.

Martin Kotora interconnects Naphthalene, Benzene derivatives, Benzaldehyde and Bond cleavage in the investigation of issues within Medicinal chemistry. As a part of the same scientific family, he mostly works in the field of Enantioselective synthesis, focusing on Lewis acids and bases and, on occasion, Benzonitrile. While the research belongs to areas of Bipyridine, Martin Kotora spends his time largely on the problem of Enantiomer, intersecting his research to questions surrounding Reaction sequence.

His most cited work include:

  • Regio- and stereoselective synthesis of γ-alkylidenebutenolides and related compounds (173 citations)
  • Cycloaddition Reaction of Zirconacyclopentadienes to Alkynes: Highly Selective Formation of Benzene Derivatives from Three Different Alkynes (158 citations)
  • Selective preparation of pyridines, pyridones, and iminopyridines from two different alkynes via azazirconacycles. (151 citations)

What are the main themes of his work throughout his whole career to date?

Martin Kotora mostly deals with Organic chemistry, Catalysis, Medicinal chemistry, Stereochemistry and Enantioselective synthesis. Martin Kotora conducted interdisciplinary study in his works that combined Organic chemistry and Metathesis. The study incorporates disciplines such as Combinatorial chemistry and Polymer chemistry in addition to Catalysis.

As a member of one scientific family, Martin Kotora mostly works in the field of Medicinal chemistry, focusing on Ring and, on occasion, Bicyclic molecule. Many of his studies involve connections with topics such as Stereoselectivity and Stereochemistry. His Enantioselective synthesis study deals with Bipyridine intersecting with Solvent.

He most often published in these fields:

  • Organic chemistry (57.67%)
  • Catalysis (57.67%)
  • Medicinal chemistry (42.02%)

What were the highlights of his more recent work (between 2015-2021)?

  • Catalysis (57.67%)
  • Enantioselective synthesis (23.93%)
  • Medicinal chemistry (42.02%)

In recent papers he was focusing on the following fields of study:

Martin Kotora mainly focuses on Catalysis, Enantioselective synthesis, Medicinal chemistry, Combinatorial chemistry and Organic chemistry. Cycloaddition, Stoichiometry and Transition metal is closely connected to Intramolecular force in his research, which is encompassed under the umbrella topic of Catalysis. His work carried out in the field of Enantioselective synthesis brings together such families of science as Aldol reaction, Aldehyde, Stereochemistry and Lewis acids and bases.

He has included themes like Ring and Bipyridine in his Medicinal chemistry study. His Combinatorial chemistry course of study focuses on Ligand and Chemical synthesis. Martin Kotora undertakes interdisciplinary study in the fields of Organic chemistry and Metathesis through his works.

Between 2015 and 2021, his most popular works were:

  • Specific Inhibitors of HIV Capsid Assembly Binding to the C-Terminal Domain of the Capsid Protein: Evaluation of 2-Arylquinazolines as Potential Antiviral Compounds (26 citations)
  • A Ruthenium Complex-Catalyzed Cyclotrimerization of Halodiynes with Nitriles. Synthesis of 2- and 3-Halopyridines (19 citations)
  • Dodecyl Amino Glucoside Enhances Transdermal and Topical Drug Delivery via Reversible Interaction with Skin Barrier Lipids (15 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Catalysis
  • Alkene

Martin Kotora mainly investigates Catalysis, Organic chemistry, Enantioselective synthesis, Medicinal chemistry and Organocatalysis. Martin Kotora has researched Catalysis in several fields, including Combinatorial chemistry, Ligand and Stereochemistry. His Combinatorial chemistry study integrates concerns from other disciplines, such as Aryl, Alkyl and 2,2'-Bipyridine.

His Stereochemistry research is multidisciplinary, incorporating elements of Brønsted–Lowry acid–base theory and Asymmetric induction. His study in Aldol reaction and Lewis acids and bases is carried out as part of his studies in Organic chemistry. His study on Organocatalysis is mostly dedicated to connecting different topics, such as Bipyridine.

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.

Best Publications

Regio- and stereoselective synthesis of γ-alkylidenebutenolides and related compounds

Ei-ichi Negishi;Martin Kotora.
Tetrahedron (1997)

263 Citations

Cycloaddition Reaction of Zirconacyclopentadienes to Alkynes: Highly Selective Formation of Benzene Derivatives from Three Different Alkynes

Tamotsu Takahashi;Zhenfeng Xi;Akiko Yamazaki;Yuanhong Liu.
Journal of the American Chemical Society (1998)

250 Citations

Selective preparation of pyridines, pyridones, and iminopyridines from two different alkynes via azazirconacycles.

Tamotsu Takahashi;Fu-Yu Tsai;Yanzhong Li;Hui Wang.
Journal of the American Chemical Society (2002)

225 Citations

Copper-Mediated Coupling of Zirconacyclopentadienes with Dihalo Aromatic Compounds. Formation of Fused Aromatic Rings

Tamotsu Takahashi;Ryuichiro Hara;Yasushi Nishihara;Martin Kotora.
Journal of the American Chemical Society (1996)

199 Citations

Carbon−Carbon Bond Formation Reaction of Zirconacyclopentadienes with Alkynes in the Presence of Ni(II)-complexes

Tamotsu Takahashi;Fu-Yu Tsai;Yanzhong Li;Kiyohiko Nakajima.
Journal of the American Chemical Society (1999)

165 Citations

Coupling reaction of zirconacyclopentadienes with dihalonaphthalenes and dihalopyridines: a new procedure for the preparation of substituted anthracenes, quinolines, and isoquinolines.

Tamotsu Takahashi;Yanzhong Li;Petr Stepnicka;Masanori Kitamura.
Journal of the American Chemical Society (2002)

153 Citations

Carbon-Carbon Bond Cleavage and Selective Transformation of Zirconacycles

Tamotsu Takahashi;Martin Kotora;Ryuichiro Hara;Zhenfeng Xi.
Bulletin of the Chemical Society of Japan (1999)

151 Citations

Selective Formation of Substituted Pyridines from Two Different Alkynes and a Nitrile: Novel Coupling Reaction of Azazirconacyclopentadienes with Alkynes

Tamotsu Takahashi;and Fu-Yu Tsai;Martin Kotora.
Journal of the American Chemical Society (2000)

144 Citations

On the Mechanism of Asymmetric Allylation of Aldehydes with Allyltrichlorosilanes Catalyzed by QUINOX, a Chiral Isoquinoline N-Oxide

Andrei V. Malkov;Pedro Ramirez-Lopez;Lada Biedermannova;Lubomir Rulisek.
Journal of the American Chemical Society (2008)

131 Citations

Highly Efficient and Selective Procedures for the Synthesis of γ-Alkylidenebutenolides via Palladium-Catalyzed Ene-Yne Coupling and Palladium- or Silver Catalyzed Lactonization of (Z)-2-En-4-ynoic Acids. Synthesis of Rubrolides A, C, D, and E

Matin Kotora;Ei-ichi Negishi.
Synthesis (1997)

111 Citations

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