Loyola University Chicago

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Loyola University Chicago

Department of Chemistry and Biochemistry

Research

Eichman, Chad

Title/s: Assistant Professor

Office #: FH-213

Phone: 773.508.3357

E-mail: ceichman@luc.edu

External Webpage: http://www.eichmangroup.com/

Degrees

Research Interests

Research in the Eichman group is focused on the development of catalytic processes that enable new reactions for organic synthesis. Expanding on this central theme, we are interested in two main areas: 1) new catalyst design for biomimetic transformations, and 2) incorporating renewable resources into complex molecule synthesis. Nature’s approach toward the synthesis of complex molecules typically involves rapid generation of advanced intermediates from relatively simple building blocks. Adopting a similar approach in a chemical synthesis laboratory is challenging and often requires the integration of novel bond construction techniques. Introducing high levels of molecular complexity in a single synthetic operation alleviates the need for long, linear synthetic sequences. Toward this goal, our primary objective is to design transition metal and metal-free catalysts for new reaction discovery. These reactions will be employed in constructing biologically active scaffolds, the testing of which will lead to collaborative chemical biology studies. Concurrently, mechanistic investigations of these processes will help increase catalyst efficiency and will ultimately fuel new catalyst discovery.

Awards

Selected Publications

Cohen, D. T.; Eichman, C. C.; Phillips, E. M.; Zarefsky, E. R.; Scheidt, K. A. “Catalytic Dynamic Kinetic Resolutions with N-Heterocyclic Carbenes: Asymmetric Synthesis of Highly Substituted β-Lactones”Angew. Chem., Int. Ed. 2012, 51, 7309.

Kunchithapatham, K.; Eichman, C. C.; Stambuli, J. P. “Synthesis of Diaryl Ketones via a Phosphine-free Fukuyama Reaction” Chem. Commun. 2011, 47, 12679.

Henderson, W. H.; Alvarez, J. M.; Eichman, C. C.; Stambuli, J. P. “Characterization, Reactivity, and Potential Catalytic Intermediacy of a Cyclometalated Tri-tert-butylphosphine Palladium Acetate Complex” Organometallics, 2011, 30, 5038.

Eichman, C. C.; Bragdon, J. P.; Stambuli, J. P. “Exploiting Guanidine as a Ligand in Cobalt-catalyzed Alkyne Cyclotrimerizations” Synlett 2011, 8, 1109.

Eichman, C. C.; Stambuli, J. P. “Transition Metal Catalyzed Synthesis of Aryl Sulfides” Molecules Invited Contribution for Special Homogenous Catalysis Issue 2011, 16, 590.

Counceller, C. M.; Eichman, C. C.; Stambuli, J. P. “Synthesis of 2,4- and 2,5-Disubstituted Oxazoles via Metal-Catalyzed Cross-Coupling Reactions” Adv. Synth. Catal. 2011, 353, 79.

Counceller, C. M.; Eichman, C. C.; Wray, B. C.; Welin, E. R.; Stambuli, J. P. “Synthesis of 3-methyl-1H-Indazole via Metal-Free Electrophilic Amination” Org. Synth. 2011, 88, 33.

Eichman, C. C.; Stambuli, J. P. “Zinc-Mediated Palladium-Catalyzed Formation of Carbon-Sulfur Bonds” J. Org. Chem. 2009, 74, 4005.

Counceller, C. M.; Eichman, C. C.; Wray, B. C.; Stambuli, J. P. “A Practical, Metal-Free Synthesis of 1H-Indazoles” Org. Lett. 2008, 10, 1021.

Loyola

Department of Chemistry & Biochemistry
Loyola University Chicago · 1032 W. Sheridan Rd., Chicago, IL 60660
Phone: 773.508.3100 · Fax: 773.508.3086

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