Yue-Lei Chen
Affiliations: | University of Minnesota, Twin Cities, Minneapolis, MN |
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"Yue-Lei Chen"Mean distance: 9.83
Parents
Sign in to add mentor| Hartmut Redlich | grad student | 2004-2007 | University of Muenster, Germany |
| Dieter Hoppe | post-doc | 2007-2009 | University of Muenster, Germany |
| Robert Vince | post-doc | 2009-2010 | UMN |
| Zhengqiang Wang | post-doc | 2009-2010 | UMN |
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Publications
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| Wang X, Su M, Li Y, et al. (2019) Tranylcypromine and 6-trifluoroethyl thienopyrimidine hybrid as LSD1 inhibitor. Bioorganic & Medicinal Chemistry Letters |
| Liu T, Tang J, Liang J, et al. (2019) Stereoselective N-glycosylation with N4-acyl cytosines and efficient synthesis of gemcitabine Tetrahedron. 75: 1203-1213 |
| Hu J, Wang Y, Li Y, et al. (2018) Structure-based optimization of a series of selective BET inhibitors containing aniline or indoline groups. European Journal of Medicinal Chemistry. 150: 156-175 |
| Liu T, Zhu Z, Ren H, et al. (2018) Efficient syntheses of alpha- and beta-C-nucleosides and the origin of anomeric selectivity Organic Chemistry Frontiers. 5: 1992-1999 |
| Liu T, Ren H, Li C, et al. (2018) Convenient preparation of pinometostat and related 5′-deoxy-5′-amino adenosine derivatives as well as their activity against DOT1L Tetrahedron Letters. 59: 415-417 |
| Liu T, Xie W, Li C, et al. (2017) Preparation of 5'-deoxy-5'-amino-5'-C-methyl adenosine derivatives and their activity against DOT1L. Bioorganic & Medicinal Chemistry Letters |
| Kirby KA, Myshakina NA, Christen MT, et al. (2017) A 2-hydroxyisoquinoline-1,3-dione active site RNase H inhibitor binds in multiple modes to HIV-1 reverse transcriptase. Antimicrobial Agents and Chemotherapy |
| Hu J, Wang Y, Li Y, et al. (2017) Discovery of a series of dihydroquinoxalin-2(1H)-ones as selective BET inhibitors from a dual PLK1-BRD4 inhibitor. European Journal of Medicinal Chemistry. 137: 176-195 |
| Tang J, Vernekar SK, Chen YL, et al. (2017) Synthesis, biological evaluation and molecular modeling of 2-Hydroxyisoquinoline-1,3-dione analogues as inhibitors of HIV reverse transcriptase associated ribonuclease H and polymerase. European Journal of Medicinal Chemistry. 133: 85-96 |
| Li Y, Liu T, Li C, et al. (2017) A one-pot synthesis of omarigliptin and its analogues through stabilized beta-amino ketone intermediate Synthetic Communications. 47: 357-363 |