David D. Ford, Ph.D.
Affiliations: | 2013 | Chemistry | Harvard University, Cambridge, MA, United States |
Area:
Mechanistic and synthetic chemistryGoogle:
"David Ford"Parents
Sign in to add mentorEric N. Jacobsen | grad student | 2013 | Harvard | |
(The Role of Catalyst-Catalyst Interactions in Asymmetric Catalysis with (salen)Cobalt(III) Complexes and Hydrogen-Bond Donors.) |
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Publications
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Akin A, Barrila MT, Brandt TA, et al. (2017) A Scalable Route for the Regio- and Enantioselective Preparation of a Tetrazole Prodrug: Application to the Multi-Gram-Scale Synthesis of a PCSK9 Inhibitor Organic Process Research & Development. 21: 1990-2000 |
Ford DD, Lehnherr D, Kennedy CR, et al. (2016) Anion-Abstraction Catalysis: The Cooperative Mechanism of α-Chloroether Activation by Dual Hydrogen-Bond Donors. Acs Catalysis. 6: 4616-4620 |
Kennedy CR, Lehnherr D, Rajapaksa NS, et al. (2016) Mechanism-Guided Development of a Highly Active Bis-Thiourea Catalyst for Anion-Abstraction Catalysis. Journal of the American Chemical Society. 138: 13525–8 |
Lehnherr D, Ford DD, Bendelsmith AJ, et al. (2016) Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity. Organic Letters. 18: 3214-7 |
Ford DD, Lehnherr D, Kennedy CR, et al. (2016) On- and Off-Cycle Catalyst Cooperativity in Anion-Binding Catalysis. Journal of the American Chemical Society. 138: 7860-3 |
Ford DD, Lehnherr D, Kennedy CR, et al. (2016) Anion-Abstraction Catalysis: The Cooperative Mechanism of α-Chloroether Activation by Dual H-Bond Donors Acs Catalysis. 6: 4616–4620 |
Ford DD, Nielsen LP, Zuend SJ, et al. (2013) Mechanistic basis for high stereoselectivity and broad substrate scope in the (salen)Co(III)-catalyzed hydrolytic kinetic resolution. Journal of the American Chemical Society. 135: 15595-608 |
Nielsen LP, Zuend SJ, Ford DD, et al. (2012) Mechanistic basis for high reactivity of (salen)Co-OTs in the hydrolytic kinetic resolution of terminal epoxides. The Journal of Organic Chemistry. 77: 2486-95 |