Lee Research Group
PUBLICATIONS
1. Koo, J.; Kim, W.; Lee, H. G. Chem. Sci. 2021, 12, 4119
"Benzylic C(sp3)–C(sp2) cross-coupling of indoles enabled by oxidative radical generation and nickel catalysis"
2. Kim, C.; Roh, B.; Lee, H. G. Chem. Sci. 2021, 12, 3668
"Restoration of catalytic activity by the preservation of ligand structure: Cu-catalysed asymmetric conjugate addition with 1,1-diborylmethane"
3. Chung, H.; Kim, J.; González-Montiel, G. A.; Cheong, P. H.-Y.; Lee, H. G. Org. Lett. 2021, 23, 1096
"Modular Counter-Fischer–Indole Synthesis through Radical-Enolate Coupling"
Previous Publications
4. Zhao, W.; Lee, H. G.; Buchwald, S. L.; Hooker, J. M. J. Am. Chem. Soc. 2017, 139, 7152.
“Direct 11CN-Labeling of Native Peptides via Palladium-Mediated Sequential Cross-Coupling Reactions.”
5. Lee, H. G.; Lautrette, G.; Pentelute. B. L.; Buchwald, S. L. Angew. Chem. Int. Ed. 2017, 56, 3177. “Palladium-mediated Arylation of Lysine in Unprotected Peptides.”
6. Lautrette, G.; Touti, F.; Lee, H. G.; Dai, P.; Pentelute, B. L. J. Am. Chem. Soc. 2016, 138, 8340.
“Nitrogen Arylation for Macrocyclization of Unprotected Peptides.”
7. Sather, A. C.; Lee, H. G.; De La Rosa, V. Y.; Yang, Y.; Muller, P.; Buchwald, S. L. J. Am. Chem. Soc. 2015, 137, 13433.
“A Fluorinated Ligand Enables Room Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides.”
8. Sather, A. C.; Lee, H. G.; Colombe, J. R.; Zhang, A. Buchwald, S. L. Nature 2015, 524, 208.
“"Dosage" Delivery of Sensitive Reagents Enables Glove Box-Free Synthesis.”
9. Lee, H. G.; Milner, P. J.; Placzek, M. S.; Buchwald, S. L.; Hooker, J. M. J. Am. Chem. Soc. 2015, 137, 648. “Virtually Instantaneous, Room-temperature [11C]-Cyanation Using Biaryl Phosphine Pd(0) Complexes.”
10. Lee, H. G.; Milner, P. J.; Colvin, M. T.; Andreas, L; Buchwald, S. L. Inorg. Chim. Acta 2014, 422, 188. “Structure and Reactivity of [(L•Pd)n•(1,5-Cyclooctadiene)] (n=1-2) Complexes Bearing Biaryl Phosphine Ligands.”
11. Lee, H. G.; Milner, P. J.; Buchwald, S. L. J. Am. Chem. Soc. 2014, 136, 3792.
“Pd-Catalyzed Nucleophilic Fluorination of Aryl Bromides.”
12. Lee, H. G.; Milner, P. J.; Buchwald, S. L. Org. Lett. 2013, 15, 5602.
“An Improved Catalyst System for the Pd-Catalyzed Fluorination of (Hetero)aryl Triflates.”
13. Lee, H. G.; Ahn, J.; Lee, A. S.; Shair, M. D. Chem. Eur. J. 2010, 16, 13058.
“Enantioselective Synthesis of the Full Carbon Skeleton of the Lomaiviticin Aglycone Reveals Remarkable Remote Substituent Effects in the Dimerization Event.”
14. Lee, D.; Lee, H. G.; Kim, S.; Yeom, C.; Kim, B. M. Adv. Synth. Catal. 2006, 348, 1021.
“A Novel Chemoentrapment Approach for Support-Free Recycling of a Catalyst: Catalytic Asymmetric Dihydroxylation.”
15. Lee, D.; Lee, J.; Lee, H. G.; Jin, S.; Hyeon, T.; Kim, B. M. Adv. Synth. Catal. 2006, 348, 41.
“Filtration-Free Recyclable Catalytic Asymmetric Dihydroxylation Using a Ligand Immobilized on Magnetic Mesocellular Mesoporous Silica.”
16. Park, J.; Lee, H. G.; Bolm, C.; Kim, B. M. Chem. Eur. J. 2005, 11, 945.
“Asymmetric Diethyl and Diphenylzinc Additions to Aldehydes by using a Fluorine-containing Chiral Amino Alcohol: A Striking Temperature Effect on the Enantioselectivity, a Minimal Amino Alcohol Loading, and an Efficient Recycling of the Amino Alcohol.”