Younggi Choi

N-Arylsulfonyl-α-amino carboxamides are potent and selective inhibitors of the chemokine receptor CCR10 that show efficacy in the murine DNFB model of contact hypersensitivity.

D. Jeanfavre, N. Moss, Jiang-Ping Wu, 2016, Bioorganic & medicinal chemistry letters.

β-Functionalization of Saturated Aza-Heterocycles Enabled by Organic Photoredox Catalysis.

David A. Nicewicz, B. Aquila, D. Nicewicz, 2021, ACS catalysis.

Piperazinyl-oxadiazoles as selective sphingosine-1-phosphate receptor agonists.

E. Hickey, Wei Xu, L. Patnaude, 2014, Bioorganic & medicinal chemistry letters.

Total synthesis of (-)- and ent-(+)-vindoline and related alkaloids.

Hayato Ishikawa, Gregory I. Elliott, Younggi Choi, 2006, Journal of the American Chemical Society.

Catalyzed Asymmetric Diels-Alder Reactions of Benzoquinone. Total Synthesis of (-)-Ibogamine

James D White, Younggi Choi, 2002 .

Total synthesis of (-)- and ent-(+)-vindoline.

Gregory I. Elliott, D. Boger, H. Ishikawa, 2005, Organic letters.

A new class of 5-HT2B antagonists possesses favorable potency, selectivity, and rat pharmacokinetic properties.

Younggi Choi, N. Moss, D. Skow, 2009, Bioorganic & medicinal chemistry letters.

Intramolecular Photocycloaddition of Unsaturated Isoquinuclidines. Synthesis of 2-Azatetracyclo[4.0.0.(4,9)0(7,10)]decanes and 3-Azatetracyclo[6.1.1.0.(2,7)0(5,9)]decanes.

James D White, Younggi Choi, 2004, Journal of Organic Chemistry.

Nickel-Catalyzed Cross-Electrophile Reductive Couplings of Neopentyl Bromides with Aryl Bromides.

C. Senanayake, N. Yee, B. Qu, 2020, The Journal of organic chemistry.