What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Aldehyde
His primary areas of study are Organic chemistry, Catalysis, Stereochemistry, Enantioselective synthesis and Stereocenter.
His work in the fields of Organic chemistry, such as Microwave irradiation, Green chemistry and Solvent, overlaps with other areas such as Chemical synthesis.
His Catalysis research is multidisciplinary, relying on both Quinoline, Iodine, Pyran, Combinatorial chemistry and Isocyanide.
Shu-Jiang Tu interconnects Cycloaddition, Azomethine ylide, Molecule, Stereoisomerism and Domino in the investigation of issues within Stereochemistry.
His biological study spans a wide range of topics, including Cascade reaction and Isatin.
His Stereocenter research includes themes of Yield, Hydrogen bond, Indoline and Povarov reaction.
His most cited work include:
- Multicomponent Reactions for the Synthesis of Heterocycles (283 citations)
- Scaffold‐Inspired Enantioselective Synthesis of Biologically Important Spiro[pyrrolidin‐3,2′‐oxindoles] with Structural Diversity through Catalytic Isatin‐Derived 1,3‐Dipolar Cycloadditions (161 citations)
- A Catalytic Asymmetric Isatin-Involved Povarov Reaction: Diastereo- and Enantioselective Construction of Spiro[indolin-3,2′-quinoline] Scaffold (140 citations)
What are the main themes of his work throughout his whole career to date?
Shu-Jiang Tu mainly focuses on Organic chemistry, Catalysis, Combinatorial chemistry, Microwave irradiation and Medicinal chemistry.
His research integrates issues of Quinoline and Aqueous medium in his study of Catalysis.
His Combinatorial chemistry research incorporates themes from Pyridine, Cascade reaction, Domino and Microwave assisted.
The study incorporates disciplines such as Yield, Acetic acid, Dimedone and Solvent in addition to Microwave irradiation.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Acridine, Ring and Hydrogen bond.
In his study, Stereoselectivity is inextricably linked to Stereochemistry, which falls within the broad field of Ring.
He most often published in these fields:
- Organic chemistry (41.80%)
- Catalysis (37.62%)
- Combinatorial chemistry (31.67%)
What were the highlights of his more recent work (between 2015-2021)?
- Catalysis (37.62%)
- Combinatorial chemistry (31.67%)
- Medicinal chemistry (17.68%)
In recent papers he was focusing on the following fields of study:
Shu-Jiang Tu mainly investigates Catalysis, Combinatorial chemistry, Medicinal chemistry, Annulation and Organic chemistry.
His work on Stereoselectivity as part of general Catalysis research is often related to Oxidative phosphorylation, thus linking different fields of science.
His Combinatorial chemistry study combines topics in areas such as Metal free, Cycloaddition, Photocatalysis and Regioselectivity.
His Medicinal chemistry research incorporates elements of Salt, Aryl, Stereocenter and Nucleophilic addition.
His Annulation study integrates concerns from other disciplines, such as Nitration, Para-quinone and Stereochemistry.
His research in Reaction conditions intersects with topics in Microwave irradiation, Indoline and Microwave heating.
Between 2015 and 2021, his most popular works were:
- Merging [2+2] Cycloaddition with Radical 1,4-Addition: Metal-Free Access to Functionalized Cyclobuta[a]naphthalen-4-ols. (106 citations)
- A new cascade halosulfonylation of 1,7-enynes toward 3,4-dihydroquinolin-2(1H)-ones via sulfonyl radical-triggered addition/6-exo-dig cyclization (83 citations)
- Recent advances in radical transformations of internal alkynes (76 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Aldehyde
Shu-Jiang Tu spends much of his time researching Catalysis, Combinatorial chemistry, Organic chemistry, Medicinal chemistry and Annulation.
His study in the field of Brønsted–Lowry acid–base theory and Cycloaddition is also linked to topics like Oxidative phosphorylation, Cleavage and Surface modification.
The various areas that Shu-Jiang Tu examines in his Combinatorial chemistry study include Photocatalysis, Regioselectivity, Halogen, Metal free and Lewis acids and bases.
His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Salt and Triple bond.
His study looks at the relationship between Annulation and topics such as Para-quinone, which overlap with Enyne, Chromane, Nucleophilic substitution, Benzofuran and Quinone methide.
His Yield study incorporates themes from Alkylation and Enantioselective synthesis.
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