Organic Chemistry Laboratory

Visible light induced reactions of quinones, <i>Bull. Korean Chem. Soc.</i> <b>2024</b> "DOI: 10.1002/bkcs.12913" (<i>Invited review article</i>)

Visible light induced reactions of quinones, Bull. Korean Chem. Soc. 2024 "DOI: 10.1002/bkcs.12913" (Invited review article)

Jang. J.; Lee. G.; Cho. E. J.*

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Electrochemical Trifluoromethylation of Alkynes: The Unique Role of DMSO as a Masking Auxiliary, <i>Chem. Sci.</i> <b>2024</b>, "DOI: 10.1039/D4SC06780K"

Electrochemical Trifluoromethylation of Alkynes: The Unique Role of DMSO as a Masking Auxiliary, Chem. Sci. 2024, "DOI: 10.1039/D4SC06780K"

Jang, J.; Hwang, H. S.; Jeong, H.; Cho, E. J.*

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Nickel-Catalyzed Regio- and Stereoselective Hydroalkylation of Allenes: Exploiting the Unique Reactivity of Diazo Compounds as an Alkylating Source, ACS Catal. 2024, 14, 16570–16576

Karmakar, U.; Bae, J.; Kim, J.; Kim, S.; Yang, W.; Cho, E. J.*

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Photosensitizer-Free Benzo[1,4]oxazin-2-one Synthesis by Continuous-Flow Photochemistry, <i>ChemSusChem</i> <b>2024</b>, e202402004

Photosensitizer-Free Benzo[1,4]oxazin-2-one Synthesis by Continuous-Flow Photochemistry, ChemSusChem 2024, e202402004

Park, E.; Tambe, S. D.; Lee, J.*; Cho, E. J.*

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Platinum-Catalyzed Deoxygenation Process of N-Acyloxyamines, <i>Synthesis </i> <b>2024</b>, "DOI: 10.1055/a-2410-2291" (<i>invited Feature Article</i>)

Platinum-Catalyzed Deoxygenation Process of N-Acyloxyamines, Synthesis 2024, "DOI: 10.1055/a-2410-2291" (invited Feature Article)

Ali, K.; Cho, E. J.*

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Understanding non-covalent interactions in Ni-catalyzed reactions: Mechanistic insights into stereoselective tetrasubstituted allene synthesis, Chem Catal. 2024, 4, 101082

Kim, S.; Lee, D. S.; Iqbal, N.; Bae, J.; Hwang, H. S.; Baek, D. H.; Hong, S.; Cho, E. J.*

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Efficient photoredox catalysis in C–C cross-coupling reactions by two-coordinated Au(I) complex, <i>Nat. Comm.</i> <b>2024</b>, <i>15</i>, 6586

Efficient photoredox catalysis in C–C cross-coupling reactions by two-coordinated Au(I) complex, Nat. Comm. 2024, 15, 6586

Jhun, B. H.; Jang, J.; Lee, S.; Cho, E. J.*; You, Y.*

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Charge-Recombinative Triplet Sensitization of Alkenes for DeMayo-type [2+2] Cycloaddition, <i>Chem. Sci.</i> <b>2024</b>, <i>15</i>, 12058-12066

Charge-Recombinative Triplet Sensitization of Alkenes for DeMayo-type [2+2] Cycloaddition, Chem. Sci. 2024, 15, 12058-12066

Lee, Y.; Jhun, B. H.; Woo, S.; Kim, S.; Bae, J.; You, Y.*; Cho, E. J.*

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Electrochemical Synthesis of Trifluoromethylated Oxazoles: Aminotrifluoromethylation of Alkynes/in-situ Cyclization, <i>Adv. Synth. Catal.</i> <b>2024</b>, <i>366</i>, 3450-3454 (Special issue : <i>Fluorine Chemistry</i>)

Electrochemical Synthesis of Trifluoromethylated Oxazoles: Aminotrifluoromethylation of Alkynes/in-situ Cyclization, Adv. Synth. Catal. 2024, 366, 3450-3454 (Special issue : Fluorine Chemistry)

Jang, J.; Cho, E. J.*

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Nickel-Catalyzed Double Deoxygenative C–N Coupling of Acyloxyamines, <i>Org. Lett.</i> <b>2024</b>, <i>26</i>, 5192–5195

Nickel-Catalyzed Double Deoxygenative C–N Coupling of Acyloxyamines, Org. Lett. 2024, 26, 5192–5195

Ali, K.; Cho, E. J.*

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Dual Photoredox and Nickel Catalysis in Regioselective Diacylation: Exploring the Versatility of Nickel Oxidation States in Allene Activation, Org. Lett. 2024, 26, 4147–4151

Tambe, S. D.; Hwang, H. S.; Park, E.; Cho, E. J.*

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Ni-catalyzed regioselective C–C bond formation of 1,1-disubstituted allenes with aldehydes, <i>Org. Chem. Front.</i> <b>2024</b>, <i>11</i>, 816-821

Ni-catalyzed regioselective C–C bond formation of 1,1-disubstituted allenes with aldehydes, Org. Chem. Front. 2024, 11, 816-821

Kim, S.; Kim, J.; Tambe, S. D.; Cho, E. J.*

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P,N Ligand in Ni-Catalyzed Cross-Coupling Reactions: A Promising Tool for Functionalization, <i>ACS Catal.</i> <b>2023</b>, <i>13</i>, 13540–13560

P,N Ligand in Ni-Catalyzed Cross-Coupling Reactions: A Promising Tool for Functionalization, ACS Catal. 2023, 13, 13540–13560

Bae, J.; Cho, E. J.*

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Boosted Heterogeneous Catalysis by Surface-Accumulated Excess Electrons of Non-Oxidized Bare Copper Nanoparticles on Electride Support, <i>Adv. Sci.</i> <b>2023</b>, <i>10</i>, e2204248

Boosted Heterogeneous Catalysis by Surface-Accumulated Excess Electrons of Non-Oxidized Bare Copper Nanoparticles on Electride Support, Adv. Sci. 2023, 10, e2204248

Han, S. S.; Thacharon, A.; Kim, J.; Chung, K.; Liu, X.; Jang, W. S.; Jetybayeva, A.; Hong, S.; Lee, K. H.; Kim, Y. M.; Cho, E. J.*, Kim, S. W.*

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Photoredox Selective Homocoupling of Propargyl Bromides, <i>J. Org. Chem.</i> <b>2023</b>, <i>88</i>, 6382-6389

Photoredox Selective Homocoupling of Propargyl Bromides, J. Org. Chem. 2023, 88, 6382-6389

Kim, S.; Lee, Y.; Cho, E. J.*

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Visible Light-Induced Metal-Free Fluoroalkylations, <i>Chem. Rec.</i> <b>2023</b>, <i>23</i>, e202300036

Visible Light-Induced Metal-Free Fluoroalkylations, Chem. Rec. 2023, 23, e202300036

Ka, C. H.; Kim, S.; Cho, E. J.*

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Construction of a Pentacyclic Framework Enabled by Nickel Catalysis, <i>Org. Lett.</i> <b>2023</b>, <i>25</i>, 647-652

Construction of a Pentacyclic Framework Enabled by Nickel Catalysis, Org. Lett. 2023, 25, 647-652

Iqbal, N.; Ashraf, M. A.; Gul, A. R.; Bae, J.; Iqbal, N.; Park, T. J.; Cho, E. J.*

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Base-free NiH-catalyzed regio- and stereo-selective hydroacylation of allenes: A new route to synthesis of tetra-substituted olefins, <i>Chem. Catal.</i> <b>2023</b>, <i>3</i>, 100606

Base-free NiH-catalyzed regio- and stereo-selective hydroacylation of allenes: A new route to synthesis of tetra-substituted olefins, Chem. Catal. 2023, 3, 100606

Bera, M.; Tambe, S. D.; Hwang, H. S.; Kim, S.; Cho, E. J.*

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Nonclassical Arylative Meyer–Schuster Rearrangement through Ni-Catalyzed Inner-Sphere Acyloxy Migration, <i>ACS Catal</i>. <b>2023</b>, <i>13</i>, 10756-10764

Nonclassical Arylative Meyer–Schuster Rearrangement through Ni-Catalyzed Inner-Sphere Acyloxy Migration, ACS Catal. 2023, 13, 10756-10764

Bae, J.; Lee, W.; Hwang, H. S.; Kim, S.; Kang, J.; Iqbal, N.*; Cho, E. J.*

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[3,3]-Rearrangements of N-Oxyindoles, <i>Synlett</i>, <b>2023</b>, <i>34</i>, 1019-1022

[3,3]-Rearrangements of N-Oxyindoles, Synlett, 2023, 34, 1019-1022

Ali, K; Bera, M.; Cho, E. J.*

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Publication

Journals

Visible light induced reactions of quinones, Bull. Korean Chem. Soc. 2024 "DOI: 10.1002/bkcs.12913" (Invited review article)

Electrochemical Trifluoromethylation of Alkynes: The Unique Role of DMSO as a Masking Auxiliary, Chem. Sci. 2024, "DOI: 10.1039/D4SC06780K"

Nickel-Catalyzed Regio- and Stereoselective Hydroalkylation of Allenes: Exploiting the Unique Reactivity of Diazo Compounds as an Alkylating Source, ACS Catal. 2024, 14, 16570–16576

Photosensitizer-Free Benzo[1,4]oxazin-2-one Synthesis by Continuous-Flow Photochemistry, ChemSusChem 2024, e202402004

Platinum-Catalyzed Deoxygenation Process of N-Acyloxyamines, Synthesis 2024, "DOI: 10.1055/a-2410-2291" (invited Feature Article)

Understanding non-covalent interactions in Ni-catalyzed reactions: Mechanistic insights into stereoselective tetrasubstituted allene synthesis, Chem Catal. 2024, 4, 101082

Efficient photoredox catalysis in C–C cross-coupling reactions by two-coordinated Au(I) complex, Nat. Comm. 2024, 15, 6586

Charge-Recombinative Triplet Sensitization of Alkenes for DeMayo-type [2+2] Cycloaddition, Chem. Sci. 2024, 15, 12058-12066

Electrochemical Synthesis of Trifluoromethylated Oxazoles: Aminotrifluoromethylation of Alkynes/in-situ Cyclization, Adv. Synth. Catal. 2024, 366, 3450-3454 (Special issue : Fluorine Chemistry)

Nickel-Catalyzed Double Deoxygenative C–N Coupling of Acyloxyamines, Org. Lett. 2024, 26, 5192–5195

Dual Photoredox and Nickel Catalysis in Regioselective Diacylation: Exploring the Versatility of Nickel Oxidation States in Allene Activation, Org. Lett. 2024, 26, 4147–4151

Ni-catalyzed regioselective C–C bond formation of 1,1-disubstituted allenes with aldehydes, Org. Chem. Front. 2024, 11, 816-821

P,N Ligand in Ni-Catalyzed Cross-Coupling Reactions: A Promising Tool for Functionalization, ACS Catal. 2023, 13, 13540–13560

Boosted Heterogeneous Catalysis by Surface-Accumulated Excess Electrons of Non-Oxidized Bare Copper Nanoparticles on Electride Support, Adv. Sci. 2023, 10, e2204248

Photoredox Selective Homocoupling of Propargyl Bromides, J. Org. Chem. 2023, 88, 6382-6389

Visible Light-Induced Metal-Free Fluoroalkylations, Chem. Rec. 2023, 23, e202300036

Construction of a Pentacyclic Framework Enabled by Nickel Catalysis, Org. Lett. 2023, 25, 647-652

Base-free NiH-catalyzed regio- and stereo-selective hydroacylation of allenes: A new route to synthesis of tetra-substituted olefins, Chem. Catal. 2023, 3, 100606

Nonclassical Arylative Meyer–Schuster Rearrangement through Ni-Catalyzed Inner-Sphere Acyloxy Migration, ACS Catal. 2023, 13, 10756-10764

[3,3]-Rearrangements of N-Oxyindoles, Synlett, 2023, 34, 1019-1022