What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Jiang Cheng mostly deals with Organic chemistry, Catalysis, Medicinal chemistry, Trifluoromethyl and Palladium.
Organic chemistry is represented through his Aryl, Cyanation, Nitrile, Aldehyde and Indole test research.
As a part of the same scientific study, Jiang Cheng usually deals with the Cyanation, concentrating on Cyanide and frequently concerns with Halogenation and Trifluoromethylation.
His Catalysis research is multidisciplinary, incorporating perspectives in Chelation, Solvent effects and Stereochemistry.
His studies deal with areas such as Ketone, Bond cleavage and Copper as well as Medicinal chemistry.
His Trifluoromethyl research focuses on Nitro and how it connects with Indolin 2 one, Peroxide and Yield.
His most cited work include:
- Palladium-catalyzed acylation of sp2 C-H bond: direct access to ketones from aldehydes. (211 citations)
- Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides (187 citations)
- The palladium-catalyzed cyanation of indole C–H bonds with the combination of NH4HCO3 and DMSO as a safe cyanide source (186 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Catalysis, Organic chemistry, Medicinal chemistry, Aryl and Palladium.
The concepts of his Catalysis study are interwoven with issues in Combinatorial chemistry, Ligand, Polymer chemistry and Copper.
His study involves Cyanation, Trifluoromethyl, Copper catalyzed, Cyanide and Peroxide, a branch of Organic chemistry.
His work is dedicated to discovering how Medicinal chemistry, Nitro are connected with Ring and other disciplines.
Jiang Cheng combines subjects such as Copper mediated, Halide, Intramolecular force and Yield with his study of Aryl.
His work carried out in the field of Palladium brings together such families of science as Chelation, Phenols and C h bond.
He most often published in these fields:
- Catalysis (59.91%)
- Organic chemistry (58.53%)
- Medicinal chemistry (41.01%)
What were the highlights of his more recent work (between 2014-2021)?
- Organic chemistry (58.53%)
- Medicinal chemistry (41.01%)
- Catalysis (59.91%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Organic chemistry, Medicinal chemistry, Catalysis, Aryl and Annulation.
In his work, Jiang Cheng performs multidisciplinary research in Organic chemistry and Ammoxidation.
His Medicinal chemistry study combines topics from a wide range of disciplines, such as Intramolecular force, Cyanation and Carbene.
As a part of the same scientific family, Jiang Cheng mostly works in the field of Cyanation, focusing on Copper catalyzed and, on occasion, Cyanide and Reaction conditions.
His Catalysis study combines topics in areas such as Combinatorial chemistry and Iodine.
The study incorporates disciplines such as Silylation, Silanes, Carboxylation and Palladium in addition to Aryl.
Between 2014 and 2021, his most popular works were:
- Palladium-Catalyzed Multi-Component Reactions of N-Tosylhydrazones, 2-Iodoanilines and CO2 towards 4-Aryl-2-Quinolinones (46 citations)
- TBAI-Catalyzed Reaction between N-Tosylhydrazones and Sulfur: A Procedure toward 1,2,3-Thiadiazole (44 citations)
- Copper-catalyzed N-cyanation of sulfoximines by AIBN. (41 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Organic chemistry, Catalysis, Medicinal chemistry, Aryl and Functional group are his primary areas of study.
His work on Organic chemistry deals in particular with Copper catalyzed, Peroxide, Cyanation and Silylation.
His Copper catalyzed research is multidisciplinary, relying on both Bond formation, Reaction conditions and Cyanide.
His research in Catalysis intersects with topics in Molecule and Sulfur.
He has included themes like Alkylation, Stereochemistry and Alkyl in his Medicinal chemistry study.
The Aryl study combines topics in areas such as Silanes, Aromaticity, Palladium, Allylic rearrangement and Carboxylation.
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