Nathaniel T. Kenton
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
16
Citations
213
Est. group size
—
Recurring co-author estimate
Active years
37
Publishing since 1989
Nathaniel T. Kenton's work focuses on the chemical synthesis and structural analysis of complex natural products, especially marine toxins like azaspiracid-3, using total synthesis to determine their precise 3D molecular structure (stereochemistry). Related work includes designing chemical tools for studying enzymes (proteolytic enzymes and methyltransferases) and developing molecules for radioactive labeling used in medical imaging (PET scans).
Publication activity shows a cluster of outputs around 2016-2017 followed by a multi-year gap and a small resurgence in 2025, indicating an irregular rather than steady publishing pattern over the last decade.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Peptidyl-Asp metalloendopeptidase
Handbook of Proteolytic Enzymes · 2025
- Stereochemical Definition of the Natural Product (6<i>R</i>,10<i>R</i>,13<i>R</i>, 14<i>R</i>,16<i>R</i>,17<i>R</i>,19<i>S</i>,20<i>S</i>,21<i>R</i>,24<i>S</i>,25<i>S</i>,28<i>S</i>,30<i>S</i>,32<i>R</i>,33<i>R</i>,34<i>R</i>,36<i>S</i>,37<i>S</i>,39<i>R</i>)‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses
Angewandte Chemie International Edition · 2017
- Total Synthesis of (6<i>R</i>,10<i>R</i>,13<i>R</i>,14<i>R</i>,16<i>R</i>,17<i>R</i>,19<i>S</i>,20<i>R</i>,21<i>R</i>,24<i>S</i>, 25<i>S</i>,28<i>S</i>,30<i>S</i>,32<i>R</i>,33<i>R</i>,34<i>R</i>,36<i>S</i>,37<i>S</i>,39<i>R</i>)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product
Angewandte Chemie International Edition · 2017
- Stereochemical Definition of the Natural Product (6<i>R</i>,10<i>R</i>,13<i>R</i>, 14<i>R</i>,16<i>R</i>,17<i>R</i>,19<i>S</i>,20<i>S</i>,21<i>R</i>,24<i>S</i>,25<i>S</i>,28<i>S</i>,30<i>S</i>,32<i>R</i>,33<i>R</i>,34<i>R</i>,36<i>S</i>,37<i>S</i>,39<i>R</i>)‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses
Angewandte Chemie · 2017
- Total Synthesis of (6<i>R</i>,10<i>R</i>,13<i>R</i>,14<i>R</i>,16<i>R</i>,17<i>R</i>,19<i>S</i>,20<i>R</i>,21<i>R</i>,24<i>S</i>, 25<i>S</i>,28<i>S</i>,30<i>S</i>,32<i>R</i>,33<i>R</i>,34<i>R</i>,36<i>S</i>,37<i>S</i>,39<i>R</i>)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product
Angewandte Chemie · 2017
- Macrocycle‐Based Hydroxamate Ligands for Complexation and Immunoconjugation of <sup>89</sup>Zirconium for Positron Emission Tomography (PET) Imaging
ChemPlusChem · 2016
- Synthesis of the C22–C40 Domain of the Azaspiracids
Organic Letters · 2016
- Capturing Unknown Substrates via <i>in Situ</i> Formation of Tightly Bound Bisubstrate Adducts: <i>S</i>-Adenosyl-vinthionine as a Functional Probe for AdoMet-Dependent Methyltransferases
Journal of the American Chemical Society · 2016
- Angewandte Chemie International Edition×2
- Angewandte Chemie×2
- Handbook of Proteolytic Enzymes×2
- ChemPlusChem×1
- Organic Letters×1
- Qi Yang
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Michael J. Holmes
Environmental Science · Purdue University West Lafayette
- Emily A. Smith
Medicine · Purdue University West Lafayette
- Edisson Tello
Agricultural and Biological Sciences · The Ohio State University
- Ravi Jangir
Chemistry · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile