What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
William H. Pearson mainly focuses on Stereochemistry, Cycloaddition, Aliphatic compound, Organic chemistry and Total synthesis.
His Stereochemistry study incorporates themes from Monoterpene and Aldol condensation.
The various areas that William H. Pearson examines in his Cycloaddition study include Intramolecular reaction and Intramolecular force.
His study looks at the relationship between Intramolecular reaction and fields such as 1,3-Dipolar cycloaddition, as well as how they intersect with chemical problems.
His Aliphatic compound research includes elements of Medicinal chemistry, Tin, Lithium, Enol ether and Stereoselectivity.
William H. Pearson studied Total synthesis and Pyrrolidine that intersect with Ring, Kopsia, Indole test, Pyrroline and Reactivity.
His most cited work include:
- Synthetic applications of 1,3-dipolar cycloaddition chemistry toward heterocycles and natural products (796 citations)
- Configurational stability of chiral, nonconjugated nitrogen-substituted organolithium compounds generated by tin-lithium exchange of N-[(1-tri-n-butylstannyl)alkyl]imidazolidin-2-ones and -oxazolidin-2-ones (114 citations)
- Pyrrolo-dC and pyrrolo-C: fluorescent analogs of cytidine and 2′-deoxycytidine for the study of oligonucleotides ☆ (111 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Stereochemistry, Medicinal chemistry, Cycloaddition, Organic chemistry and Intramolecular force.
William H. Pearson has included themes like Ring and Swainsonine in his Stereochemistry study.
His studies in Medicinal chemistry integrate themes in fields like Iminium, Transmetalation, Alkyl and Amine gas treating.
His Cycloaddition research is multidisciplinary, relying on both Azide, Total synthesis, Indolizidines and Pyrrolidine.
His research in Intramolecular force intersects with topics in Ion, Yield, 1,3-Dipolar cycloaddition and Schmidt reaction.
His Aliphatic compound research includes themes of Stereoselectivity, Benzaldehyde, Lithium and Asymmetric induction.
He most often published in these fields:
- Stereochemistry (39.05%)
- Medicinal chemistry (36.69%)
- Cycloaddition (36.69%)
What were the highlights of his more recent work (between 2002-2011)?
- Stereochemistry (39.05%)
- Organic chemistry (30.18%)
- Cycloaddition (36.69%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Stereochemistry, Organic chemistry, Cycloaddition, Reagent and Medicinal chemistry.
His Total synthesis, Tropane and Indole test study in the realm of Stereochemistry interacts with subjects such as Chemical synthesis.
His study connects Intramolecular force and Cycloaddition.
His work deals with themes such as Indolizidines, Ketone, Yield and One-pot synthesis, which intersect with Intramolecular force.
The concepts of his Reagent study are interwoven with issues in Combinatorial chemistry, Tin and Triazene.
His research investigates the connection between Medicinal chemistry and topics such as Aryl that intersect with issues in Allylic rearrangement.
Between 2002 and 2011, his most popular works were:
- Pyrrolo-dC and pyrrolo-C: fluorescent analogs of cytidine and 2′-deoxycytidine for the study of oligonucleotides ☆ (111 citations)
- Total synthesis of the Kopsia lapidilecta alkaloid (+/-)-lapidilectine B. (79 citations)
- Fluorous affinity purification of oligonucleotides. (64 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of investigation include Stereochemistry, Cycloaddition, Intramolecular force, Chemical synthesis and Total synthesis.
His research integrates issues of Golgi apparatus, Biochemistry and Kifunensine in his study of Stereochemistry.
His work is dedicated to discovering how Cycloaddition, Indole test are connected with Imine, Ring and Intramolecular reaction and other disciplines.
The Intramolecular force study combines topics in areas such as Yield, Ketone, Alkylation and Azomethine ylide.
His Total synthesis research integrates issues from Pyrrolidine, Reactivity, Aryl, Alkyl and Kopsia.
His Pyrrolidine study deals with the bigger picture of Medicinal chemistry.
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