Mikail E Abbasov, Ph.D.
Affiliations: | 2021- | Department of Chemistry and Chemical Biology | Cornell University, Ithaca, NY, United States |
Area:
Chemical Biology, Molecular Medicine, Synthetic Chemistry, Cell/Molecular BiologyWebsite:
https://www.chemikailproteomics.com/Google:
"Mikail Abbasov"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Daniel Romo | grad student | Texas A & M | |
| Benjamin F. Cravatt | post-doc | Scripps Institute |
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Publications
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| Abbasov ME, Kavanagh ME, Ichu TA, et al. (2021) Publisher Correction: A proteome-wide atlas of lysine-reactive chemistry. Nature Chemistry |
| Abbasov ME, Kavanagh ME, Ichu TA, et al. (2021) A proteome-wide atlas of lysine-reactive chemistry. Nature Chemistry |
| Chaheine CM, Gladen PT, Abbasov ME, et al. (2020) Enantioselective, Organocatalytic Strategy for the Oxazolomycin Core: Formal Synthesis of (+)-Neooxazolomycin. Organic Letters |
| Alvariño R, Alonso E, Abbasov ME, et al. (2019) Gracilin A derivatives target early events in Alzheimer's disease: effects on neuroinflammation and oxidative stress. Acs Chemical Neuroscience |
| Abbasov ME, Alvariño R, Chaheine CM, et al. (2019) Simplified immunosuppressive and neuroprotective agents based on gracilin A. Nature Chemistry. 11: 342-350 |
| Abbasov ME, Hudson BM, Tantillo DJ, et al. (2017) Stereodivergent, Diels-Alder-initiated organocascades employing α,β-unsaturated acylammonium salts: scope, mechanism, and application. Chemical Science. 8: 1511-1524 |
| Abbasov ME, Hudson BM, Kong W, et al. (2017) Enantioselective Diels-Alder-lactamization organocascades employing a furan-based diene. Organic & Biomolecular Chemistry |
| Abbasov ME, Romo D. (2014) The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis. Natural Product Reports. 31: 1318-27 |
| Abbasov ME, Hudson BM, Tantillo DJ, et al. (2014) Acylammonium salts as dienophiles in Diels-Alder/lactonization organocascades. Journal of the American Chemical Society. 136: 4492-5 |