Alan M. Hyde
Affiliations: | Merck, Rahway, NJ |
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"Alan Michael Hyde"Bio:
http://hdl.handle.net/1721.1/49746
Mean distance: 7.29 | S | N | B | C | P |
Parents
Sign in to add mentor| Stephen L. Buchwald | grad student | 2009 | MIT | |
| (The development and synthetic applications of Ti- and Pd-catalyzed processes) | ||||
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Publications
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| Klapars A, Chung JYL, Limanto J, et al. (2021) Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036 |
| Orr RK, McCabe Dunn JM, Nolting A, et al. (2018) New reactions and processes for the efficient synthesis of a HCV NS5b prodrug Green Chemistry. 20: 2519-2525 |
| Banik SM, Levina A, Hyde AM, et al. (2017) Lewis acid enhancement by hydrogen-bond donors for asymmetric catalysis. Science (New York, N.Y.). 358: 761-764 |
| Klausen RS, Kennedy CR, Hyde AM, et al. (2017) Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction. Journal of the American Chemical Society |
| He CQ, Simon A, Lam YH, et al. (2017) A Model for the Enantioselectivity of Asymmetric Intramolecular Alkylations by bis-Quaternized Cinchona Alkaloid-Derived Catalysts. The Journal of Organic Chemistry |
| Ji Y, Li H, Hyde AM, et al. (2017) A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions. Chemical Science. 8: 2841-2851 |
| DiRocco DA, Ji Y, Sherer EC, et al. (2017) A multifunctional catalyst that stereoselectively assembles prodrugs. Science (New York, N.Y.). 356: 426-430 |
| 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 |
| Li H, Belyk KM, Yin J, et al. (2015) Enantioselective Synthesis of Hemiaminals via Pd-Catalyzed C-N Coupling with Chiral Bisphosphine Mono-Oxides. Journal of the American Chemical Society |
| Beck EM, Hyde AM, Jacobsen EN. (2011) Chiral sulfinamide/achiral sulfonic acid cocatalyzed enantioselective protonation of enol silanes. Organic Letters. 13: 4260-3 |