Masahiro Terada focuses on Catalysis, Enantioselective synthesis, Organic chemistry, Brønsted–Lowry acid–base theory and Phosphoric acid. His work carried out in the field of Catalysis brings together such families of science as Combinatorial chemistry and Stereochemistry. His research in Enantioselective synthesis intersects with topics in Guanidine, Hemiaminal and Ene reaction.
The Yield, Amination, Aryl and Stereoisomerism research Masahiro Terada does as part of his general Organic chemistry study is frequently linked to other disciplines of science, such as Glyoxylate cycle, therefore creating a link between diverse domains of science. His Phosphoric acid research is multidisciplinary, relying on both Redox and Metal. His research integrates issues of Electrophile, Acetyl acetone and Mannich reaction in his study of Homogeneous catalysis.
Catalysis, Organic chemistry, Enantioselective synthesis, Medicinal chemistry and Brønsted–Lowry acid–base theory are his primary areas of study. His biological study spans a wide range of topics, including Guanidine, Phosphoric acid, Polymer chemistry, Stereochemistry and Combinatorial chemistry. His study in the fields of Enantiomer, Cycloaddition, Diels–Alder reaction and Aldol reaction under the domain of Organic chemistry overlaps with other disciplines such as Glyoxylate cycle.
In his work, Titanium is strongly intertwined with Ene reaction, which is a subfield of Enantioselective synthesis. His studies examine the connections between Medicinal chemistry and genetics, as well as such issues in Copper catalyzed, with regards to Cleavage. His work is dedicated to discovering how Brønsted–Lowry acid–base theory, Brook rearrangement are connected with Umpolung and other disciplines.
His scientific interests lie mostly in Catalysis, Brønsted–Lowry acid–base theory, Medicinal chemistry, Enantioselective synthesis and Combinatorial chemistry. Catalysis is the subject of his research, which falls under Organic chemistry. His Brønsted–Lowry acid–base theory research is multidisciplinary, incorporating elements of Cycloaddition, Allylic rearrangement, Alkene, Brook rearrangement and Addition reaction.
His Medicinal chemistry study combines topics from a wide range of disciplines, such as Aryl, Intramolecular force and Nucleophile. His Enantioselective synthesis study combines topics in areas such as Electrophile, Phosphoric acid and Substitution reaction. The Combinatorial chemistry study combines topics in areas such as Molecule, Nucleophilic addition and Organic synthesis.
Masahiro Terada mainly focuses on Catalysis, Enantioselective synthesis, Brønsted–Lowry acid–base theory, Combinatorial chemistry and Medicinal chemistry. Catalysis is a primary field of his research addressed under Organic chemistry. The study incorporates disciplines such as Hydrogen bond, Moiety, Allylic rearrangement and Addition reaction in addition to Enantioselective synthesis.
The concepts of his Brønsted–Lowry acid–base theory study are interwoven with issues in Brook rearrangement and Cycloaddition. His Combinatorial chemistry research includes elements of Nucleophilic addition and Organic synthesis. His Medicinal chemistry research focuses on Intramolecular force and how it connects with Carbene, Alkoxy group and Copper catalyzed.
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Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation.
Daisuke Uraguchi;Masahiro Terada.
Journal of the American Chemical Society (2004)
Chiral Phosphoric Acids asVersatile Catalysts for Enantioselective Transformations
Masahiro Terada.
Synthesis (2010)
Binaphthol-derived phosphoric acid as a versatile catalyst for enantioselective carbon–carbon bond forming reactions
Masahiro Terada.
Chemical Communications (2008)
Catalytic asymmetric glyoxylate-ene reaction: a practical access to .alpha.-hydroxy esters in high enantiomeric purities
Koichi Mikami;Masahiro Terada;Takeshi Nakai.
Journal of the American Chemical Society (1990)
Enantioselective friedel-crafts reaction of electron-rich alkenes catalyzed by chiral brønsted acid
Masahiro Terada;Keiichi Sorimachi.
Journal of the American Chemical Society (2007)
Organocatalytic Asymmetric Aza-Friedel−Crafts Alkylation of Furan
Daisuke Uraguchi;Keiichi Sorimachi;Masahiro Terada.
Journal of the American Chemical Society (2004)
High Substrate/Catalyst Organocatalysis by a Chiral Brønsted Acid for an Enantioselective Aza‐Ene‐Type Reaction
Masahiro Terada;Kyoko Machioka;Keiichi Sorimachi.
Angewandte Chemie (2006)
Axially chiral guanidine as enantioselective base catalyst for 1,4-addition reaction of 1,3-dicarbonyl compounds with conjugated nitroalkenes.
Masahiro Terada;Hitoshi Ube;Yusuke Yaguchi.
Journal of the American Chemical Society (2006)
Axially chiral guanidine as highly active and enantioselective catalyst for electrophilic amination of unsymmetrically substituted 1,3-dicarbonyl compounds.
Masahiro Terada;Megumi Nakano;Hitoshi Ube.
Journal of the American Chemical Society (2006)
Conformationally Flexible Biphenyl‐phosphane Ligands for Ru‐Catalyzed Enantioselective Hydrogenation
Koichi Mikami;Toshinobu Korenaga;Masahiro Terada;Takeshi Ohkuma.
Angewandte Chemie (1999)
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