2016 - Ryoji Noyori Prize, Society of Synthetic Organic Chemistry
Keiji Maruoka mostly deals with Organic chemistry, Catalysis, Enantioselective synthesis, Combinatorial chemistry and Aldehyde. Organic chemistry is closely attributed to Medicinal chemistry in his study. His Catalysis study deals with Phase intersecting with Michael reaction.
Keiji Maruoka interconnects Amino acid, Aldol reaction, Ammonium, Mannich reaction and Reactivity in the investigation of issues within Enantioselective synthesis. Homogeneous catalysis is closely connected to Electrophile in his research, which is encompassed under the umbrella topic of Combinatorial chemistry. His Aldehyde research is multidisciplinary, incorporating elements of Chiral Lewis acid and Amine gas treating.
Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Medicinal chemistry are his primary areas of study. His Catalysis research includes themes of Amino acid and Phase. His is involved in several facets of Organic chemistry study, as is seen by his studies on Reagent, Aldol reaction, Lewis acids and bases, Stereoselectivity and Aldehyde.
His Lewis acids and bases research includes elements of Denticity, Polymer chemistry and Organic synthesis. His studies in Enantioselective synthesis integrate themes in fields like Schiff base, Stereochemistry, Glycine and Ammonium. His Bifunctional research extends to Combinatorial chemistry, which is thematically connected.
His primary scientific interests are in Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Organocatalysis. His work on Alkylation as part of general Catalysis study is frequently connected to Conjugate, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His Enantioselective synthesis research is multidisciplinary, incorporating perspectives in Imine, Amide, Optically active, Phase-transfer catalyst and Stereoselectivity.
His biological study deals with issues like Copper catalyzed, which deal with fields such as Alkyl radicals. His research in Organocatalysis intersects with topics in Amino acid and Electrophile. His work in Medicinal chemistry addresses subjects such as Nucleophile, which are connected to disciplines such as Intramolecular force.
The scientist’s investigation covers issues in Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Reagent. The various areas that Keiji Maruoka examines in his Catalysis study include Hydrogen bond, Medicinal chemistry and Ammonium. His research integrates issues of Bifunctional, Phase, Michael reaction and Stereoselectivity in his study of Enantioselective synthesis.
Keiji Maruoka has included themes like Copper catalyzed, Phase-transfer catalyst and Primary in his Combinatorial chemistry study. The study incorporates disciplines such as Nanotechnology and Manganese in addition to Reagent. His Organocatalysis study combines topics in areas such as Amino acid and Enantiomer.
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.
Enantioselective amino acid synthesis by chiral phase-transfer catalysis.
Keiji Maruoka;Takashi Ooi.
Chemical Reviews (2003)
Recent development and application of chiral phase-transfer catalysts.
Takuya Hashimoto;Keiji Maruoka.
Chemical Reviews (2007)
Recent advances in asymmetric phase-transfer catalysis.
Takashi Ooi;Keiji Maruoka.
Angewandte Chemie (2007)
Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions
Takuya Hashimoto;Keiji Maruoka.
Chemical Reviews (2015)
Recent Developments in Asymmetric Phase-Transfer Reactions
Seiji Shirakawa;Keiji Maruoka.
Angewandte Chemie (2013)
Molecular Design of a C2-Symmetric Chiral Phase-Transfer Catalyst for Practical Asymmetric Synthesis of α-Amino Acids
Takashi Ooi;and Minoru Kameda;Keiji Maruoka.
Journal of the American Chemical Society (1999)
Design of N-Spiro C2-Symmetric Chiral Quaternary Ammonium Bromides as Novel Chiral Phase-Transfer Catalysts: Synthesis and Application to Practical Asymmetric Synthesis of α-Amino Acids
Takashi Ooi;Minoru Kameda;Keiji Maruoka.
Journal of the American Chemical Society (2003)
Asymmetric hetero-Diels-Alder reaction catalyzed by a chiral organoaluminum reagent
Keiji. Maruoka;Takayuki. Itoh;Tadashi. Shirasaka;Hisashi. Yamamoto.
Journal of the American Chemical Society (1988)
Practical Catalytic Enantioselective Synthesis of α,α-Dialkyl-α-amino Acids by Chiral Phase-Transfer Catalysis
Takashi Ooi;Mifune Takeuchi;and Minoru Kameda;Keiji Maruoka.
Journal of the American Chemical Society (2000)
Phosphonium Salts as Chiral Phase‐Transfer Catalysts: Asymmetric Michael and Mannich Reactions of 3‐Aryloxindoles
Rongjun He;Changhua Ding;Keiji Maruoka.
Angewandte Chemie (2009)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: