Calcium(II)-catalyzed enantioselective conjugate additions of amines

Methodology

Uno, B. E.; Dicken, R. D.; Redfern, L. R.; Stern, C. M.; Krzywicki, G. G.; Scheidt, K. A.*Chem. Sci. 2018, 9, 1634-1639.

A Cooperative Ternary Catalysis System for Asymmetric Lactonizations of α-Ketoesters

Methodology

Murauski, K. J. R.; Walden, D. M.; Cheong, P. H-Y.; Scheidt, K. A.* Adv. Synth. Catal. 2017, 359, 3713-3719. https://doi.org/10.1002/adsc.201701015 Featured in: Yamamoto, H.; Shimoda, Y. Synfacts 2018, 14 (02), 0163.

Formation of Aza-ortho-quinone Methides Under Room Temperature Conditions: Cs₂CO₃ Effect

Methodology

Walden, D. M.; Johnston, R. C.; Jaworski, A. A.; Hovey, M. T.; Meyer, M. P.; Scheidt, K. A.* and Cheong, P. H.* J. Org. Chem. 2017, 82, 7183-7189  

Catalytic, Enantioselective β-Protonation through a Cooperative Activation Strategy

Methodology

Wang , M.; Barsoum , D.; Schwamb , C. B.; Cohen, D. T.; Goess , B. C.; Riedrich , M.; Chan, A.; Maki, B. E.; Mishra, R. K.; Scheidt , K. A.* J. Org. Chem. 2017, 82, 4689-4702. https://doi.org/10.1021/acs.joc.7b00334

A Biocatalytic Route to Highly Enantioenriched β-Hydroxydioxinones

Methodology

Betori, R. C.; Miller, E. R.; Scheidt, K. A., Adv. Synth. Cat. 2017, 359, 1131-1137.

Cooperative Catalysis and Activation with N-Heterocyclic Carbenes

Methodology

Wang, M. H.; Scheidt, K. A., Angew. Chem. Int. Ed. 2016, 5, 424-429.