Artis Klapars, Ph.D.
Affiliations: | 2000 | University of Wisconsin, Madison, Madison, WI |
Area:
organic synthesisGoogle:
"Artis Klapars"Mean distance: 8.34 | S | N | B | C | P |
Parents
Sign in to add mentorEdwin Vedejs | grad student | 2000 | UW Madison | |
(Enantiocontrolled synthesis of an aziridinomitosene.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Zultanski SL, Kuhl N, Zhong W, et al. (2020) Mechanistic Understanding of a Robust and Scalable Synthesis of Per(6-deoxy-6-halo)cyclodextrins, Versatile Intermediates for Cyclodextrin Modification Organic Process Research & Development |
DiRocco DA, Ji Y, Sherer EC, et al. (2017) A multifunctional catalyst that stereoselectively assembles prodrugs. Science (New York, N.Y.). 356: 426-430 |
Simmons B, Liu Z, Klapars A, et al. (2017) Mechanism-Based Solution to the ProTide Synthesis Problem: Selective Access to Sofosbuvir, Acelarin, and INX-08189. Organic Letters |
Hyde AM, Liu Z, Kosjek B, et al. (2016) Synthesis of the GPR40 Partial Agonist MK-8666 through a Kinetically Controlled Dynamic Enzymatic Ketone Reduction. Organic Letters |
Chung JY, Shevlin M, Klapars A, et al. (2016) Asymmetric Synthesis of N-Boc-(R)-Silaproline via Rh-Catalyzed Intramolecular Hydrosilylation of Dehydroalanine and Continuous Flow N-Alkylation. Organic Letters |
Limanto J, Ashley ER, Yin J, et al. (2014) A highly efficient asymmetric synthesis of vernakalant. Organic Letters. 16: 2716-9 |
Mangion IK, Chen CY, Li H, et al. (2014) Enantioselective synthesis of an HCV NS5a antagonist. Organic Letters. 16: 2310-3 |
Maddess ML, Scott JP, Alorati A, et al. (2014) Enantioselective synthesis of a highly substituted tetrahydrofluorene derivative as a potent and selective estrogen receptor beta agonist Organic Process Research and Development. 18: 528-538 |
Barker G, McGrath JL, Klapars A, et al. (2011) Enantioselective, palladium-catalyzed α-arylation of N-Boc pyrrolidine: in situ react IR spectroscopic monitoring, scope, and synthetic applications. The Journal of Organic Chemistry. 76: 5936-53 |
Yasuda N, Klapars A, Kohmura Y, et al. (2011) Asymmetric synthesis of a potent hNK-1 receptor antagonist Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 69: 579-587 |