What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Enzyme
- Catalysis
His primary areas of investigation include Stereochemistry, Organic chemistry, Catalysis, Crystallography and Lactam.
His work on Nucleoside is typically connected to Glucosidase Inhibitor as part of general Stereochemistry study, connecting several disciplines of science.
His work in the fields of Organic chemistry, such as Dehydrogenation, In situ, Reagent and Toluene, intersects with other areas such as Substitution.
The various areas that Spencer Knapp examines in his Catalysis study include Aryl and Total synthesis.
The study incorporates disciplines such as Nickel, Zinc, Ring and Porphyrin in addition to Crystallography.
Spencer Knapp interconnects Indolizidines, Indolizidine, Radical cyclization, Bicyclic molecule and Carboxamide in the investigation of issues within Lactam.
His most cited work include:
- Synthesis of Complex Nucleoside Antibiotics (246 citations)
- Crystallographic evidence for substrate-assisted catalysis in a bacterial beta-hexosaminidase. (207 citations)
- NAG-thiazoline, An N-Acetyl-β-hexosaminidase Inhibitor That Implicates Acetamido Participation (191 citations)
What are the main themes of his work throughout his whole career to date?
Stereochemistry, Organic chemistry, Medicinal chemistry, Crystallography and Nucleoside are his primary areas of study.
His primary area of study in Stereochemistry is in the field of Disaccharide.
His Organic chemistry study often links to related topics such as Nucleic acid.
His research integrates issues of Iodide and Alkyl in his study of Medicinal chemistry.
Spencer Knapp combines subjects such as Ligand and Copper with his study of Crystallography.
The concepts of his Nucleophile study are interwoven with issues in Reagent and Anomer.
He most often published in these fields:
- Stereochemistry (46.74%)
- Organic chemistry (27.72%)
- Medicinal chemistry (11.96%)
What were the highlights of his more recent work (between 2006-2020)?
- Stereochemistry (46.74%)
- Organic chemistry (27.72%)
- Medicinal chemistry (11.96%)
In recent papers he was focusing on the following fields of study:
Spencer Knapp mainly focuses on Stereochemistry, Organic chemistry, Medicinal chemistry, Glycosylation and Cycloaddition.
The various areas that Spencer Knapp examines in his Stereochemistry study include Electrophile and Active site.
In the field of Medicinal chemistry, his study on N-methylimidazole and Substituent overlaps with subjects such as Extramural.
In Glycosylation, Spencer Knapp works on issues like Nucleophile, which are connected to Indole test.
He interconnects Reactivity and Diastereomer in the investigation of issues within Cycloaddition.
His Nucleoside study combines topics from a wide range of disciplines, such as Glycosyl and Moiety.
Between 2006 and 2020, his most popular works were:
- (+)-SJ733, a clinical candidate for malaria that acts through ATP4 to induce rapid host-mediated clearance of Plasmodium (144 citations)
- A Mitotic GlcNAcylation/Phosphorylation Signaling Complex Alters the Posttranslational State of the Cytoskeletal Protein Vimentin (131 citations)
- Trans- and cis-stilbene polyphenols induced rapid perinuclear mitochondrial clustering and p53-independent apoptosis in cancer cells but not normal cells. (51 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Enzyme
- Catalysis
His scientific interests lie mostly in Stereochemistry, Cell biology, Stereoisomerism, Electrophile and Molecule.
His research in Stereochemistry intersects with topics in Active site and Chitinase.
His work on O-GlcNAcase and Phosphorylation as part of general Cell biology research is often related to Gene isoform and Cancer cell, thus linking different fields of science.
His Stereoisomerism study incorporates themes from Cyclopentane, Steric effects and Turn.
His studies deal with areas such as Fragmentation, Hexosaminidase, Enzyme and Tautomer as well as Electrophile.
His Molecule research incorporates themes from Yield and Medicinal chemistry, N-methylimidazole.
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