Kishore Thalluri
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
32
Citations
491
Est. group size
—
Recurring co-author estimate
Active years
15
Publishing since 2011
Kishore Thalluri works in synthetic and structural chemistry, developing new chemical reagents and methods for building compounds such as ureas, carbamates, and peptide derivatives. The research includes designing efficient synthesis reactions (for example, using Lossen rearrangement) and characterizing molecular structures through crystallography, including studies of enzyme-inhibitor complexes relevant to biochemistry.
Publication activity was highest around 2016-2017 and has been sparse since, averaging under one paper per year over the last five years.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- Structural Characterization of 5-Substituted Pyrrolo[3,2-<i>d</i>]pyrimidine Antifolate Inhibitors in Complex with Human Serine Hydroxymethyl Transferase 2
Biochemistry · 2024
- 2‐(tert‐ブトキシカルボニルオキシイミノ)‐2‐シアノ酢酸エチル(Boc‐Oxyma):Lossen転位によるラセミ化フリーのウレア化合物,カルバマートおよびチオカルバマート合成のための効率的試薬
Advanced Synthesis & Catalysis · 2017
- CCDC 1484427: Experimental Crystal Structure Determination
The Cambridge Structural Database · 2017
- Ethyl 2‐(<i>tert</i>‐Butoxycarbonyloxyimino)‐2‐cyanoacetate (Boc‐Oxyma): An Efficient Reagent for the Racemization Free Synthesis of Ureas, Carbamates and Thiocarbamates via Lossen Rearrangement
Advanced Synthesis & Catalysis · 2016
- Benzoxazole and Benzothiazole Synthesis from Carboxylic Acids in Solution and on Resin by Using Ethyl 2‐Cyano‐2‐(2‐nitrobenzenesulfonyloxyimino)acetate and <i>para</i>‐Toluenesulfonic Acid
Asian Journal of Organic Chemistry · 2016
- ChemInform Abstract: Benzoxazole and Benzothiazole Synthesis from Carboxylic Acids in Solution and on Resin by Using Ethyl 2‐Cyano‐2‐(2‐nitrobenzenesulfonyloxyimino)acetate and para‐Toluenesulfonic Acid.
ChemInform · 2016
- ChemInform Abstract: Racemization Free Longer N‐Terminal Peptide Hydroxamate Synthesis on Solid Support Using Ethyl 2‐(tert‐Butoxycarbonyloxyimino)‐2‐cyanoacetate.
ChemInform · 2016
- Advanced Synthesis & Catalysis×2
- ChemInform×2
- Cell×1
- Asian Journal of Organic Chemistry×1
- Organic Letters×1
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 11, 2026.
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