Publications
167
Citations
4,388
Est. group size
~7
Recurring co-author estimate
Active years
21
Publishing since 2006
Mingji Dai's research focuses on organic chemistry, particularly the total synthesis of complex natural products (molecules found in nature, often with biological activity) using innovative chemical reactions such as radical cyclizations and C–H functionalization (methods to build molecular frameworks by selectively activating carbon-hydrogen bonds). His work often connects new synthetic methods to biological applications, including cancer immunology and inflammatory disease treatment. Prospective students would likely engage in designing efficient routes to synthesize challenging natural molecules and exploring their biological properties.
Publication output has been relatively steady over the past decade, with some fluctuation (a peak around 2020-2021) and a modest decline in the most recent years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Seven-Step Total Synthesis of Conidiogenone B Enabled by Radical Cyclizations
Journal of the American Chemical Society · 2026
- Advancing Total Synthesis Through Skeletal Editing
Accounts of Chemical Research · 2025
- MGAT1-Guided complex N-Glycans on CD73 regulate immune evasion in triple-negative breast cancer
Nature Communications · 2025
- Total Synthesis of (−)-Psathyrin A Enabled by Radical Cyclization
Journal of the American Chemical Society · 2025
- Total Synthesis of (−)-Illisimonin A Enabled by Pattern Recognition and Olefin Transposition
Journal of the American Chemical Society · 2025
- Total Synthesis of (−)-Neocucurbol C Enabled by Pattern Recognition and MHAT Cyclization
Journal of the American Chemical Society · 2025
- Light-Regulated Agonists Spatiotemporally Activating the Vitamin D Receptor Mitigate Psoriasis-like Inflammation in Mice without Inducing Hypercalcemia
ACS Central Science · 2025
- Reverse polarity of amide nitrogen enables expedient access to N-cyano amides
Nature Communications · 2025
- Comparative analysis of complanadine A total syntheses
Beilstein Journal of Organic Chemistry · 2025
- Total Synthesis of (±)-Phaeocaulisin A Enabled Chemistry Innovation and Biological Discovery
Synlett · 2025
- Convergent and Efficient Total Synthesis of (+)-Heilonine Enabled by C–H Functionalizations
Journal of the American Chemical Society · 2024
- Tuning Immune‐Cold Tumor by Suppressing USP10/B7‐H4 Proteolytic Axis Reinvigorates Therapeutic Efficacy of ADCs
Advanced Science · 2024
- Ten-Step Total Synthesis of (±)-Phaeocaulisin A Enabled by Cyclopropanol Ring-Opening Carbonylation
Journal of the American Chemical Society · 2024
- Concise Total Syntheses of (<i>−</i>)-Crinipellins A and B Enabled by a Controlled Cargill Rearrangement
Journal of the American Chemical Society · 2024
- S<sub>N</sub>2 Reaction at the Amide Nitrogen Center Enables Hydrazide Synthesis
Angewandte Chemie International Edition · 2024
- The Cambridge Structural Database×20
- Journal of the American Chemical Society×18
- Angewandte Chemie International Edition×6
- Angewandte Chemie×6
- Nature Communications×5
- Shivakrishna Kallepu
Chemistry · Purdue University West Lafayette
- David R. Williams
Chemistry · Indiana University
- Arun K. Ghosh
Chemistry · Purdue University West Lafayette
- Seth A. Bawel
Chemistry · Indiana 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 20, 2026.
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