Timothy J. Senter
Affiliations: | 2015- | Chemistry | Massachusetts Institute of Technology, Cambridge, MA, United States |
Website:
http://web.mit.edu/chemistry/buchwald/people/profiles-postdoc.html#senterGoogle:
"Timothy James Senter"Bio:
https://www.linkedin.com/pub/timothy-senter/35/642/3a2
https://events.vanderbilt.edu/index.php?eID=56714
Mean distance: 7.2 | S | N | B | C | P |
Parents
Sign in to add mentor| Larry G. French | research assistant | 2009-2010 | St. Lawrence University | |
| Craig W. Lindsley | grad student | 2010-2015 | Vanderbilt | |
| (A General and Stereoselective Approach for the Construction of Nitrogen-Containing Heterocycles: Application Towards the Total Synthesis of Alkaloid Natural Products) | ||||
| Stephen L. Buchwald | post-doc | 2015- | MIT | |
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Publications
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| Wexler RP, Nuhant P, Senter TJ, et al. (2019) Electrochemically Enabled Chan-Lam Couplings of Aryl Boronic Acids and Anilines. Organic Letters |
| Park NH, Senter TJ, Buchwald SL. (2016) Rapid Synthesis of Aryl Fluorides in Continuous Flow through the Balz-Schiemann Reaction. Angewandte Chemie (International Ed. in English). 55: 11907-11 |
| Senter TJ, O'Reilly MC, Chong KM, et al. (2015) A general, enantioselective synthesis of N-alkyl terminal aziridines and C2-functionalized azetidines via organocatalysis. Tetrahedron Letters. 56: 1276-1279 |
| Senter T, Gogliotti RD, Han C, et al. (2015) Progress towards small molecule menin-mixed lineage leukemia (MLL) interaction inhibitors with in vivo utility. Bioorganic & Medicinal Chemistry Letters. 25: 2720-5 |
| Senter TJ, O'Reilly MC, Chong KM, et al. (2015) A general, enantioselective synthesis of N-alkyl terminal aziridines and C2-functionalized azetidines via organocatalysis Tetrahedron Letters. 56: 1276-1279 |
| He S, Senter TJ, Pollock J, et al. (2014) High-affinity small-molecule inhibitors of the menin-mixed lineage leukemia (MLL) interaction closely mimic a natural protein-protein interaction. Journal of Medicinal Chemistry. 57: 1543-56 |
| Grembecka JE, He S, Senter TJ, et al. (2014) Abstract 2534: High-affinity small molecule inhibitors of the menin-MLL interaction reverse oncogenic transformation mediated by MLL fusion proteins in leukemia Cancer Research. 74: 2534-2534 |
| Senter TJ, Schulte ML, Konkol LC, et al. (2013) A General, Enantioselective Synthesis of 1-Azabicyclo[m.n.0]alkane Ring Systems. Tetrahedron Letters. 54: 1645-1648 |
| Fadeyi OO, Senter TJ, Hahn KN, et al. (2012) A versatile enantioselective synthesis of azabicyclic ring systems: a concise total synthesis of (+)-grandisine D and unnatural analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5826-31 |
| Senter TJ, Fadeyi OO, Lindsley CW. (2012) Enantioselective total synthesis of (+)-amabiline. Organic Letters. 14: 1869-71 |