What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Organic chemistry, Catalysis, Medicinal chemistry, Stereochemistry and Stereoselectivity are his primary areas of study.
His work in Reagent, Allylic rearrangement, Alkylation, Ketone and Halide is related to Organic chemistry.
His Catalysis course of study focuses on Alcohol and Ion-exchange resin, Nuclear chemistry, Sulfonic acid and Acetophenone.
His Medicinal chemistry study incorporates themes from Adduct, Iodide, Alkyl and Regioselectivity.
His Stereochemistry study combines topics from a wide range of disciplines, such as Selectivity, Reactivity and Farnesol.
Hitosi Nozaki focuses mostly in the field of Stereoselectivity, narrowing it down to topics relating to Combinatorial chemistry and, in certain cases, Electrophile.
His most cited work include:
- Grignard-type carbonyl addition of allyl halides by means of chromous salt. A chemospecific synthesis of homoallyl alcohols (307 citations)
- Novel template effects of distannoxane catalysts in highly efficient transesterification and esterification (270 citations)
- Selective grignard-type carbonyl addition of alkenyl halides mediated by chromium(II) chloride (228 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Organic chemistry, Medicinal chemistry, Stereochemistry, Catalysis and Reagent.
His study in Organic chemistry concentrates on Aliphatic compound, Allylic rearrangement, Stereoselectivity, Alkylation and Ketone.
His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Adduct, Ring, Regioselectivity and Chloride.
Particularly relevant to Palladium is his body of work in Catalysis.
His work on Halide expands to the thematically related Reagent.
He most often published in these fields:
- Organic chemistry (47.45%)
- Medicinal chemistry (32.75%)
- Stereochemistry (16.67%)
What were the highlights of his more recent work (between 1982-2010)?
- Organic chemistry (47.45%)
- Catalysis (13.53%)
- Medicinal chemistry (32.75%)
In recent papers he was focusing on the following fields of study:
Hitosi Nozaki mainly focuses on Organic chemistry, Catalysis, Medicinal chemistry, Aliphatic compound and Reagent.
Aldehyde, Allylic rearrangement, Ketone, Stereoselectivity and Acetal are the core of his Organic chemistry study.
Hitosi Nozaki usually deals with Catalysis and limits it to topics linked to Stereochemistry and Aziridine.
Hitosi Nozaki has researched Medicinal chemistry in several fields, including Chromium, Dichloromethane, Lewis acids and bases and Regioselectivity.
Hitosi Nozaki interconnects Alcohol, Intramolecular reaction, Bicyclic molecule and Nuclear magnetic resonance spectroscopy in the investigation of issues within Aliphatic compound.
His research in Reagent focuses on subjects like Enol, which are connected to Halide, Structural isomer and Diol.
Between 1982 and 2010, his most popular works were:
- Novel template effects of distannoxane catalysts in highly efficient transesterification and esterification (270 citations)
- Selective grignard-type carbonyl addition of alkenyl halides mediated by chromium(II) chloride (228 citations)
- Synthesis of substituted furans by palladium-catalyzed cyclization of acetylenic ketones (158 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Hitosi Nozaki spends much of his time researching Organic chemistry, Catalysis, Aliphatic compound, Medicinal chemistry and Reagent.
Aldehyde, Ketone, Intramolecular reaction, Lewis acids and bases and Transesterification are among the areas of Organic chemistry where Hitosi Nozaki concentrates his study.
His Aliphatic compound research is multidisciplinary, incorporating perspectives in Carboxylic acid, Silicon, Alcohol, Inorganic chemistry and Nuclear magnetic resonance spectroscopy.
His Medicinal chemistry research is multidisciplinary, relying on both Stereochemistry and Regioselectivity.
His Reagent study combines topics in areas such as Yield and Allylic rearrangement.
His Palladium research integrates issues from Photochemistry and Acetonitrile.
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