What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Yong-Qiang Tu mostly deals with Organic chemistry, Catalysis, Semipinacol rearrangement, Stereochemistry and Total synthesis.
His work in Catalysis tackles topics such as Amine gas treating which are related to areas like Noble metal, Alkyne and A3 coupling reaction.
His research integrates issues of Yield, Allylic rearrangement and Stereocenter in his study of Semipinacol rearrangement.
Stereochemistry and Tandem are two areas of study in which Yong-Qiang Tu engages in interdisciplinary research.
His Total synthesis research is multidisciplinary, incorporating elements of Combinatorial chemistry, Allylic alcohol and Molecule.
The various areas that Yong-Qiang Tu examines in his Enantioselective synthesis study include Carbon and Brønsted–Lowry acid–base theory.
His most cited work include:
- Direct Sp3α-C-H activation and functionalization of alcohol and ether. (335 citations)
- Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water. (237 citations)
- Semipinacol rearrangement in natural product synthesis. (236 citations)
What are the main themes of his work throughout his whole career to date?
Yong-Qiang Tu spends much of his time researching Stereochemistry, Organic chemistry, Catalysis, Semipinacol rearrangement and Combinatorial chemistry.
His Stereochemistry research integrates issues from Stereocenter and Stereoselectivity.
His Stereoselectivity research includes themes of Diol and Ring.
His Catalysis research incorporates themes from Pyrrolidine, Medicinal chemistry and Yield.
His Semipinacol rearrangement research includes elements of Electrophile, Allylic rearrangement, Intermolecular force, Quaternary carbon and Cascade reaction.
The Allylic rearrangement study combines topics in areas such as Substrate and Silylation.
He most often published in these fields:
- Stereochemistry (45.51%)
- Organic chemistry (41.32%)
- Catalysis (43.71%)
What were the highlights of his more recent work (between 2015-2021)?
- Catalysis (43.71%)
- Combinatorial chemistry (23.95%)
- Semipinacol rearrangement (32.93%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Catalysis, Combinatorial chemistry, Semipinacol rearrangement, Total synthesis and Organic chemistry.
His biological study focuses on Enantioselective synthesis.
His studies in Combinatorial chemistry integrate themes in fields like Copper catalyzed, Stereocenter and Quinone.
While the research belongs to areas of Semipinacol rearrangement, Yong-Qiang Tu spends his time largely on the problem of Allylic rearrangement, intersecting his research to questions surrounding Substrate, Silylation, Cascade reaction and Aryl.
His Total synthesis research is included under the broader classification of Stereochemistry.
His study in Stereochemistry is interdisciplinary in nature, drawing from both Quaternary carbon, Ring and Mannich reaction.
Between 2015 and 2021, his most popular works were:
- Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis (47 citations)
- Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis (47 citations)
- Electrochemical Semipinacol Rearrangements of Allylic Alcohols: Construction of All-Carbon Quaternary Stereocenters. (27 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Total synthesis, Combinatorial chemistry, Catalysis, Semipinacol rearrangement and Enantioselective synthesis are his primary areas of study.
His Total synthesis research is under the purview of Stereochemistry.
As part of one scientific family, Yong-Qiang Tu deals mainly with the area of Catalysis, narrowing it down to issues related to the Pyrrolidine, and often Oxazoline and Ligand.
Yong-Qiang Tu interconnects Quaternary carbon, Ring, Allylic rearrangement and Nicholas reaction in the investigation of issues within Semipinacol rearrangement.
A large part of his Enantioselective synthesis studies is devoted to Stereocenter.
In his works, he undertakes multidisciplinary study on Structural diversity and Organic chemistry.
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