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Drug Discovery & Organic Synthesis Lab
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Drug Discovery & Organic Synthesis Lab
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Drug Discovery & Organic Synthesis Lab
E-mail : hongorg@kaist.ac.kr
Tel : +82-42-350-2811
Web: http://ddnpslab.kaist.ac.kr
Office : Room 4103, Department of Chemistry (Bldg E6-4),
KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Korea
Lab : Room 4118, (+82-42-350-2851, 5811)
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193.
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192.
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191. Reductive Deaminative Cross-Coupling of Alkyl Bistriflimides Enabled by ElectrocatalysisTao, X.; Lee, W.; Xu, Z.; Shu, H.; Wang, Q.; Ni, S.; Pan, Y.; Hong, S.*; Wang, Y.*2024, in press.
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190. Divergent Enantioselective Access to Diverse Chiral Compounds from Bicyclo[1.1.0]butanes and α,β-Unsaturated Ketones under Catalyst ControlJeong, J.; Cao, S.: Kang, H.-J; Yoon, H. ; Lee, J. ; Shin, S.; Kim, D.; Hong, S.*J. Am. Chem. Soc. 2024, 146, 27830.
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189. Harnessing the Potential of Acyl Triazoles in Bifunctional Cobalt-Catalyzed Radical Cross-Coupling ReactionsTan, C.-Y; Hong, S.*Nature Commun. 2024, 15, 6965.
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188. Insight into C4 Selectivity in the Light-Driven C–H Fluoroalkylation of Pyridines and QuinolinesKim, L.; Lee, W.; Hong, S.*Angew. Chem. Int. Ed. 2024, e202410408.
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187. Traceless Nucleophile Strategy for C5-Selective C–H Sulfonylation of PyridinesKim, J.; Kim, Y.-E.; Hong, S.*Angew. Chem. Int. Ed. 2024, e202409561.
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186. Iron-Hydride Catalyzed Hydropyridylation of Various Alkenes: A New Path to 1,3-Difunctionalization of [1.1.1]Propellane Kim, C.; Kim, Y.; Hong, S.* Nature Commun. 2024, 15, 5993.
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185. Nickel-Catalyzed Regio- and Enantioselective Hydrofluorination in Unactivated AlkenesKim, M.; Han, S.; Hong, S.*Synlett. 2024, 35, A-F (Invited Synpact)
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184.
