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Karl A. Scheidt grad student 2008-2013 Northwestern
 (Annulation Strategies in N-Heterocyclic Carbene-Catalysis.)
Stephen L. Buchwald post-doc 2013- MIT
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Publications

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Cohen DT, Zhang C, Fadzen CM, et al. (2018) A chemoselective strategy for late-stage functionalization of complex small molecules with polypeptides and proteins. Nature Chemistry
Scheidt K, Hovey T, Cohen D, et al. (2017) A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. Angewandte Chemie (International Ed. in English)
Wang MH, Barsoum D, Schwamb CB, et al. (2017) Catalytic, Enantioselective β-Protonation through a Cooperative Activation Strategy. The Journal of Organic Chemistry
Cohen DT, Zhang C, Pentelute BL, et al. (2015) An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides. Journal of the American Chemical Society. 137: 9784-7
Wang MH, Cohen DT, Schwamb CB, et al. (2015) Enantioselective β-Protonation by a Cooperative Catalysis Strategy. Journal of the American Chemical Society. 137: 5891-4
Cohen DT, Johnston RC, Rosson NT, et al. (2015) Functionalized cyclopentenes through a tandem NHC-catalyzed dynamic kinetic resolution and ambient temperature decarboxylation: mechanistic insight and synthetic application. Chemical Communications (Cambridge, England). 51: 2690-3
Cohen DT, Buchwald SL. (2015) Mild palladium-catalyzed cyanation of (hetero)aryl halides and triflates in aqueous media. Organic Letters. 17: 202-5
Cohen DT, Zhang C, Pentelute BL, et al. (2015) An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides Journal of the American Chemical Society. 137: 9784-9787
Johnston RC, Cohen DT, Eichman CC, et al. (2014) Catalytic Kinetic Resolution of a Dynamic Racemate: Highly Stereoselective β-Lactone Formation by N-Heterocyclic Carbene Catalysis. Chemical Science (Royal Society of Chemistry : 2010). 5: 1974-1982
Cohen DT, Eichman CC, Phillips EM, et al. (2013) Corrigendum: Catalytic Dynamic Kinetic Resolutions with N-Heterocyclic Carbenes: Asymmetric Synthesis of Highly Substituted β-Lactones Angewandte Chemie International Edition. 52: 5203-5203
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