D-Index & Metrics Best Publications

D-Index & Metrics

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 72 Citations 14,859 378 World Ranking 2318 National Ranking 148

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

Hideki Yorimitsu spends much of his time researching Organic chemistry, Catalysis, Medicinal chemistry, Palladium and Aryl. Organic chemistry is represented through his Halide, Reagent, Allylic rearrangement, Regioselectivity and Alcohol research. His study in Catalysis is interdisciplinary in nature, drawing from both Cobalt and Polymer chemistry.

His studies deal with areas such as Ether, Adduct and Alkyl as well as Medicinal chemistry. His biological study spans a wide range of topics, including Combinatorial chemistry, Reaction conditions, Indole test and Microwave irradiation. Hideki Yorimitsu has researched Aryl in several fields, including Oxidative addition, Sulfanyl, Helicene and Sulfur.

His most cited work include:

  • Cobalt-catalyzed Heck-type reaction of alkyl halides with styrenes. (164 citations)
  • Nickel-catalyzed carboxylation of organozinc reagents with CO2. (154 citations)
  • Cobalt-Catalyzed Trimethylsilylmethylmagnesium-Promoted Radical Alkenylation of Alkyl Halides: A Complement to the Heck Reaction (144 citations)

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

Hideki Yorimitsu focuses on Catalysis, Organic chemistry, Medicinal chemistry, Aryl and Palladium. His Catalysis research incorporates elements of Reagent, Polymer chemistry, Cobalt, Halide and Alkyl. His Reagent research is multidisciplinary, incorporating perspectives in Hydride, Triethylborane, Gallium trichloride, Gallium and Combinatorial chemistry.

His study in Stereoselectivity, Allylic rearrangement, Nickel, Chloride and Organic synthesis is done as part of Organic chemistry. His work carried out in the field of Medicinal chemistry brings together such families of science as Yield, Alcohol, Ether and Silylation. Hideki Yorimitsu regularly ties together related areas like Carbene in his Aryl studies.

He most often published in these fields:

  • Catalysis (51.58%)
  • Organic chemistry (46.37%)
  • Medicinal chemistry (35.80%)

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

  • Catalysis (51.58%)
  • Medicinal chemistry (35.80%)
  • Aryl (23.66%)

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

His primary areas of study are Catalysis, Medicinal chemistry, Aryl, Organic chemistry and Palladium. Hideki Yorimitsu interconnects Combinatorial chemistry, Organosulfur compounds, Borylation and Polymer chemistry in the investigation of issues within Catalysis. His Combinatorial chemistry research incorporates themes from Reagent, Intramolecular force, Benzene and Photoredox catalysis.

His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Regioselectivity, Alkylation, Nucleophile and Alkyl. Hideki Yorimitsu has researched Aryl in several fields, including Electrophile, Sulfur, Carbene, Coupling and Chloride. While the research belongs to areas of Palladium, Hideki Yorimitsu spends his time largely on the problem of Transmetalation, intersecting his research to questions surrounding Non-covalent interactions.

Between 2015 and 2021, his most popular works were:

  • Metal-Free Approach to Biaryls from Phenols and Aryl Sulfoxides by Temporarily Sulfur-Tethered Regioselective C–H/C–H Coupling (81 citations)
  • Asymmetric Alkylation of N-Sulfonylbenzamides with Vinyl Ethers via C-H Bond Activation Catalyzed by Hydroxoiridium/Chiral Diene Complexes. (55 citations)
  • Cascades of Interrupted Pummerer Reaction-Sigmatropic Rearrangement. (44 citations)

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

  • Organic chemistry
  • Catalysis
  • Alkene

His scientific interests lie mostly in Catalysis, Medicinal chemistry, Organic chemistry, Aryl and Palladium. His research in Catalysis intersects with topics in Nickel, Organosulfur compounds and Intramolecular force, Stereochemistry, Benzofuran. The various areas that he examines in his Medicinal chemistry study include Yield, Alkylation, Ring, Reactivity and Hydrogen bond.

As part of his studies on Organic chemistry, Hideki Yorimitsu often connects relevant areas like Fluorescence. His Aryl research includes elements of Combinatorial chemistry, Electrophile, Coupling and Carbene. His Palladium study combines topics from a wide range of disciplines, such as Methyl triflate and Borylation.

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

Cobalt-catalyzed Heck-type reaction of alkyl halides with styrenes.

Yousuke Ikeda;Tomoaki Nakamura;Hideki Yorimitsu;Koichiro Oshima.
Journal of the American Chemical Society (2002)

249 Citations

Nickel-catalyzed carboxylation of organozinc reagents with CO2.

Hidenori Ochiai;Minsul Jang;Koji Hirano;Hideki Yorimitsu.
Organic Letters (2008)

233 Citations

Powerful solvent effect of water in radical reaction: Triethylborane-induced atom-transfer radical cyclization in water

Hideki Yorimitsu;Tomoaki Nakamura;Hiroshi Shinokubo;Koichiro Oshima.
Journal of the American Chemical Society (2000)

226 Citations

Recent Progress in Asymmetric Allylic Substitutions Catalyzed by Chiral Copper Complexes

Hideki Yorimitsu;Koichiro Oshima.
Angewandte Chemie (2005)

215 Citations

Cobalt-Catalyzed Trimethylsilylmethylmagnesium-Promoted Radical Alkenylation of Alkyl Halides: A Complement to the Heck Reaction

Walter Affo;Hirohisa Ohmiya;Takuma Fujioka;Yousuke Ikeda.
Journal of the American Chemical Society (2006)

213 Citations

Cobalt‐Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard Reagents

Takashi Tsuji;Hideki Yorimitsu;Koichiro Oshima.
Angewandte Chemie (2002)

205 Citations

Cobalt-catalyzed tandem radical cyclization and cross-coupling reaction: Its application to benzyl-substituted heterocycles

Katsuyu Wakabayashi;Hideki Yorimitsu;Koichiro Oshima.
Journal of the American Chemical Society (2001)

203 Citations

Cobalt(diamine)-catalyzed cross-coupling reaction of alkyl halides with arylmagnesium reagents: stereoselective constructions of arylated asymmetric carbons and application to total synthesis of AH13205.

Hirohisa Ohmiya;Hideki Yorimitsu;Koichiro Oshima.
Journal of the American Chemical Society (2006)

192 Citations

Stereoselective hydrothiolation of alkynes catalyzed by cesium base: Facile access to (Z)-1-alkenyl sulfides

Azusa Kondoh;Kazuaki Takami;Hideki Yorimitsu;Koichiro Oshima.
Journal of Organic Chemistry (2005)

176 Citations

Cobalt-catalyzed cross-coupling reactions of alkyl halides with allylic and benzylic Grignard reagents and their application to tandem radical cyclization/cross-coupling reactions.

Hirohisa Ohmiya;Takashi Tsuji;Hideki Yorimitsu;Koichiro Oshima.
Chemistry: A European Journal (2004)

168 Citations

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Profile was last updated on December 6th, 2021.
Research.com Ranking is based on data retrieved from the Microsoft Academic Graph (MAG).
The ranking d-index is inferred from publications deemed to belong to the considered discipline.

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