What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
The scientist’s investigation covers issues in Organic chemistry, Catalysis, Enantioselective synthesis, BINAP and Medicinal chemistry.
His work on Aliphatic compound, Hydroformylation, Bicyclic molecule and Allylic rearrangement as part of general Organic chemistry research is frequently linked to Homogeneous, thereby connecting diverse disciplines of science.
His research investigates the connection between Catalysis and topics such as Enantiomer that intersect with issues in Nuclear magnetic resonance spectroscopy and Ligand.
His studies deal with areas such as Isoquinoline and Homogeneous catalysis as well as Enantioselective synthesis.
The BINAP study combines topics in areas such as Computational chemistry and Ruthenium.
His Medicinal chemistry research is multidisciplinary, relying on both Rhodium and Stereochemistry.
His most cited work include:
- BINAP: an efficient chiral element for asymmetric catalysis (854 citations)
- Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of .alpha.-(acylamino)acrylic acids (670 citations)
- Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity (534 citations)
What are the main themes of his work throughout his whole career to date?
Hidemasa Takaya focuses on Catalysis, Medicinal chemistry, Organic chemistry, Asymmetric hydrogenation and BINAP.
His Catalysis study frequently draws parallels with other fields, such as Optically active.
His Medicinal chemistry research incorporates elements of Ligand, Allylic rearrangement, Stereochemistry, Alkyl and Isomerization.
His Organic chemistry research focuses on subjects like Polymer chemistry, which are linked to Carbon–carbon bond.
His BINAP research integrates issues from Enantiomeric excess, Ruthenium, Triethylamine, Asymmetric induction and Stereoselectivity.
His biological study spans a wide range of topics, including Cationic polymerization, Absolute configuration and Isoquinoline.
He most often published in these fields:
- Catalysis (48.10%)
- Medicinal chemistry (40.00%)
- Organic chemistry (37.62%)
What were the highlights of his more recent work (between 1996-2010)?
- Catalysis (48.10%)
- Medicinal chemistry (40.00%)
- Hydroformylation (10.00%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Catalysis, Medicinal chemistry, Hydroformylation, Organic chemistry and Ligand.
Hidemasa Takaya has researched Catalysis in several fields, including Optically active and Styrene.
Hidemasa Takaya interconnects Enantiomer, Stereochemistry and Alkyl in the investigation of issues within Medicinal chemistry.
His study of Asymmetric hydrogenation is a part of Organic chemistry.
The Asymmetric hydrogenation study combines topics in areas such as Metalation and BINAP.
His work deals with themes such as Nuclear magnetic resonance spectroscopy and Palladium, which intersect with Ligand.
Between 1996 and 2010, his most popular works were:
- Highly Enantioselective Hydroformylation of Olefins Catalyzed by Rhodium(I) Complexes of New Chiral Phosphine−Phosphite Ligands (275 citations)
- ASYMMETRIC HYDROFORMYLATION OF OLEFINS IN A HIGHLY CROSS-LINKED POLYMER MATRIX (122 citations)
- Mechanistic Aspects of the Alternating Copolymerization of Propene with Carbon Monoxide Catalyzed by Pd(II) Complexes of Unsymmetrical Phosphine−Phosphite Ligands (120 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His main research concerns Catalysis, Hydroformylation, Organic chemistry, Phosphine and Medicinal chemistry.
His Catalysis research focuses on Styrene and how it relates to Regioselectivity and Polymer chemistry.
Hidemasa Takaya works in the field of Organic chemistry, namely Ligand.
His studies deal with areas such as Denticity and Stereochemistry as well as Phosphine.
His work in Medicinal chemistry is not limited to one particular discipline; it also encompasses Enantioselective synthesis.
His research in Enantioselective synthesis intersects with topics in Absolute configuration and Enantiomer.
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