Seung Hwan Cho, Ph.D. - Publications

2014- Chemistry Pohang University of Science and Technology (POSTECH), Pohang, Gyeongsangbuk-do, South Korea 

45 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Kim H, Jung Y, Cho SH. Defluorinative C-C Bond-Forming Reaction of Trifluoromethyl Alkenes with -(Diborylalkyl)lithiums. Organic Letters. 24: 2705-2710. PMID 35380841 DOI: 10.1021/acs.orglett.2c00809  0.3
2021 Lee Y, Han S, Cho SH. Catalytic Chemo- and Enantioselective Transformations of -Diborylalkanes and (Diborylmethyl)metallic Species. Accounts of Chemical Research. PMID 34612034 DOI: 10.1021/acs.accounts.1c00455  0.331
2020 Lim S, Cho H, Jeong J, Jang M, Kim H, Cho SH, Lee E. Cobalt-Catalyzed Defluorosilylation of Aryl Fluorides via Grignard Reagent Formation. Organic Letters. PMID 32903016 DOI: 10.1021/Acs.Orglett.0C02752  0.372
2020 Jo W, Baek SY, Hwang C, Heo J, Baik MH, Cho SH. ZnMe-Mediated, Direct Alkylation of Electron Deficient -Heteroarenes with 1,1-Diborylalkanes: Scope and Mechanism. Journal of the American Chemical Society. PMID 32605373 DOI: 10.1021/Jacs.0C06827  0.378
2020 Shin M, Kim M, Hwang C, Lee H, Kwon H, Park J, Lee E, Cho SH. Facile Synthesis of α-Boryl-Substituted Allylboronate Esters Using Stable Bis[(pinacolato)boryl]methylzinc Reagents. Organic Letters. PMID 32149519 DOI: 10.1021/Acs.Orglett.0C00721  0.38
2019 Dutta S, Kumari N, Dubbu S, Jang SW, Kumar A, Ohtsu H, Kim J, Kawano M, Cho SH, Lee IS. Highly Mesoporous Metal Organic Frameworks as Synergistic Multimodal Catalytic Platforms for Divergent Cascade Reactions. Angewandte Chemie (International Ed. in English). PMID 31880381 DOI: 10.1002/Anie.201916578  0.382
2019 Lee H, Lee Y, Cho SH. Palladium-Catalyzed Chemoselective Negishi Cross-Coupling of Bis[(pinacolato)boryl]methylzinc Halides with Aryl (Pseudo)Halides. Organic Letters. PMID 31329446 DOI: 10.1021/Acs.Orglett.9B02050  0.392
2019 Kim J, Shin M, Cho SH. Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters Acs Catalysis. 9: 8503-8508. DOI: 10.1021/Acscatal.9B02931  0.326
2019 Kim J, Hwang C, Kim Y, Cho SH. Improved Synthesis of β-Aminoboronate Esters via Copper-Catalyzed Diastereo- and Enantioselective Addition of 1,1-Diborylalkanes to Acyclic Arylaldimines Organic Process Research & Development. 23: 1663-1668. DOI: 10.1021/Acs.Oprd.9B00179  0.404
2019 Kim J, Lee E, Cho SH. Chemoselective Palladium‐Catalyzed Suzuki‐Miyaura Cross‐Coupling of (Diborylmethyl)silanes with Alkenyl Bromides Asian Journal of Organic Chemistry. 8: 1664-1667. DOI: 10.1002/Ajoc.201900328  0.403
2018 Lee Y, Park J, Cho SH. Generation and Application of (Diborylmethyl)zinc(II) Species: Access to Enantioenriched gem-Diborylalkanes by an Asymmetric Allylic Substitution. Angewandte Chemie (International Ed. in English). PMID 29964367 DOI: 10.1002/Anie.201805476  0.387
2018 Kim J, Cho SH. Access to Enantioenriched Benzylic 1,1-Silylboronate Esters by Palladium-Catalyzed Enantiotopic-Group Selective Suzuki–Miyaura Coupling of (Diborylmethyl)silanes with Aryl Iodides Acs Catalysis. 9: 230-235. DOI: 10.1021/Acscatal.8B03979  0.439
2018 Singh AK, Kim M, Lee H, Singh R, Cho SH, Kim D. Direct Aryl-Aryl Coupling without Pre-Functionalization Enabled by Excessive Oxidation of Two-Electron Ag(I)/Ag(III) Catalyst Advanced Synthesis & Catalysis. 360: 2032-2042. DOI: 10.1002/Adsc.201800213  0.306
2017 Park J, Choi S, Lee Y, Cho SH. Chemo- and Stereoselective Crotylation of Aldehydes and Cyclic Aldimines with Allylic gem-Diboronate Ester. Organic Letters. PMID 28723104 DOI: 10.1021/Acs.Orglett.7B01821  0.412
2017 Kim J, Ko K, Cho SH. Diastereo- and Enantioselective Synthesis of β-Aminoboronate Esters by Copper(I)-Catalyzed 1,2-Addition of 1,1-Bis[(pinacolato)boryl]alkanes to Imines. Angewandte Chemie (International Ed. in English). PMID 28700820 DOI: 10.1002/Anie.201705829  0.407
2017 Hwang C, Jo W, Cho SH. Base-promoted, deborylative secondary alkylation of N-heteroaromatic N-oxides with internal gem-bis[(pinacolato)boryl]alkanes: a facile derivatization of 2,2'-bipyridyl analogues. Chemical Communications (Cambridge, England). PMID 28636030 DOI: 10.1039/C7Cc03731G  0.355
2016 Lee Y, Baek SY, Park J, Kim ST, Tussupbayev S, Kim J, Baik MH, Cho SH. Chemoselective Coupling of 1,1-Bis[(pinacolato)boryl]alkanes for the Transition-Metal-Free Borylation of Aryl and Vinyl Halides: A Combined Experimental and Theoretical Investigation. Journal of the American Chemical Society. PMID 27973774 DOI: 10.1021/Jacs.6B11757  0.413
2016 Jo W, Kim J, Choi S, Cho SH. Transition-Metal-Free Regioselective Alkylation of Pyridine N-Oxides Using 1,1-Diborylalkanes as Alkylating Reagents. Angewandte Chemie (International Ed. in English). PMID 27351367 DOI: 10.1002/Anie.201603329  0.387
2016 Park J, Lee Y, Kim J, Cho SH. Copper-Catalyzed Diastereoselective Addition of Diborylmethane to N-tert-Butanesulfinyl Aldimines: Synthesis of β-Aminoboronates. Organic Letters. PMID 26900647 DOI: 10.1021/Acs.Orglett.6B00376  0.404
2016 Larsen MA, Cho SH, Hartwig JF. Iridium-Catalyzed, Hydrosilyl-Directed Borylation of Unactivated Alkyl C-H Bonds. Journal of the American Chemical Society. PMID 26745739 DOI: 10.1021/Jacs.5B12153  0.525
2015 Kim J, Park S, Park J, Cho SH. Synthesis of Branched Alkylboronates by Copper-Catalyzed Allylic Substitution Reactions of Allylic Chlorides with 1,1-Diborylalkanes. Angewandte Chemie (International Ed. in English). PMID 26666468 DOI: 10.1002/Anie.201509840  0.448
2015 Park JO, Cho SH, Lee JS, Lee W, Lee SY. A foolproof method for phase transfer of metal nanoparticles via centrifugation. Chemical Communications (Cambridge, England). PMID 26659005 DOI: 10.1039/C5Cc09344A  0.332
2015 Kim HO, Yang YS, Ko HC, Kim GM, Cho SH, Seo YJ, Son SW, Lee JR, Lee JS, Chang SE, Che JW, Park CW. Maintenance Therapy of Facial Seborrheic Dermatitis with 0.1% Tacrolimus Ointment. Annals of Dermatology. 27: 523-30. PMID 26512166 DOI: 10.5021/ad.2015.27.5.523  0.305
2015 Chung SH, Jeon DG, Cho WH, Song WS, Kong CB, Cho SH, Kim BS, Lee SY. Temporary hemiarthroplasty with a synthetic device in children with osteosarcoma around the knee as a bridging procedure until skeletal maturity. Journal of Surgical Oncology. PMID 26179818 DOI: 10.1002/jso.23964  0.324
2014 Cho SH, Hartwig JF. Iridium-catalyzed diborylation of benzylic C-H bonds directed by a hydrosilyl group: Synthesis of 1,1-benzyldiboronate esters Chemical Science. 5: 694-698. DOI: 10.1039/C3Sc52824C  0.546
2013 Cho SH, Hartwig JF. Iridium-catalyzed borylation of secondary benzylic C-H bonds directed by a hydrosilane. Journal of the American Chemical Society. 135: 8157-60. PMID 23682736 DOI: 10.1021/Ja403462B  0.547
2012 Kim JY, Park SH, Ryu J, Cho SH, Kim SH, Chang S. Rhodium-catalyzed intermolecular amidation of arenes with sulfonyl azides via chelation-assisted C-H bond activation. Journal of the American Chemical Society. 134: 9110-3. PMID 22624801 DOI: 10.1021/Ja303527M  0.538
2012 Ryu J, Cho SH, Chang S. A versatile rhodium(I) catalyst system for the addition of heteroarenes to both alkenes and alkynes by a C-H bond activation. Angewandte Chemie (International Ed. in English). 51: 3677-81. PMID 22383453 DOI: 10.1002/Anie.201200120  0.48
2012 Kim HJ, Cho SH, Chang S. Intramolecular oxidative diamination and aminohydroxylation of olefins under metal-free conditions. Organic Letters. 14: 1424-7. PMID 22364422 DOI: 10.1021/Ol300166Q  0.49
2011 Kim HJ, Kim J, Cho SH, Chang S. Intermolecular oxidative C-N bond formation under metal-free conditions: control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation. Journal of the American Chemical Society. 133: 16382-5. PMID 21928852 DOI: 10.1021/Ja207296Y  0.487
2011 Cho SH, Kim JY, Kwak J, Chang S. Recent advances in the transition metal-catalyzed twofold oxidative C-H bond activation strategy for C-C and C-N bond formation. Chemical Society Reviews. 40: 5068-83. PMID 21643614 DOI: 10.1039/C1Cs15082K  0.516
2011 Cho SH, Yoon J, Chang S. Intramolecular oxidative C-N bond formation for the synthesis of carbazoles: comparison of reactivity between the copper-catalyzed and metal-free conditions. Journal of the American Chemical Society. 133: 5996-6005. PMID 21446710 DOI: 10.1021/Ja111652V  0.551
2010 Kim JY, Cho SH, Joseph J, Chang S. Cobalt- and manganese-catalyzed direct amination of azoles under mild reaction conditions and the mechanistic details. Angewandte Chemie (International Ed. in English). 49: 9899-903. PMID 21105037 DOI: 10.1002/Anie.201005922  0.472
2009 Cho SH, Kim JY, Lee SY, Chang S. Silver-mediated direct amination of benzoxazoles: tuning the amino group source from formamides to parent amines. Angewandte Chemie (International Ed. in English). 48: 9127-30. PMID 19856358 DOI: 10.1002/Anie.200903957  0.519
2008 Hwang SJ, Cho SH, Chang S. Synthesis of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of pyrroles. Journal of the American Chemical Society. 130: 16158-9. PMID 18998684 DOI: 10.1021/Ja806897H  0.517
2008 Cho SH, Hwang SJ, Chang S. Palladium-catalyzed C-H functionalization of pyridine N-oxides: highly selective alkenylation and direct arylation with unactivated arenes. Journal of the American Chemical Society. 130: 9254-6. PMID 18582040 DOI: 10.1021/Ja8026295  0.515
2008 Lee JM, Park EJ, Cho SH, Chang S. Cu-facilitated C-O bond formation using N-hydroxyphthalimide: efficient and selective functionalization of benzyl and allylic C-H bonds. Journal of the American Chemical Society. 130: 7824-5. PMID 18512912 DOI: 10.1021/Ja8031218  0.537
2008 Cho SH, Chang S. Room temperature copper-catalyzed 2-functionalization of pyrrole rings by a three-component coupling reaction. Angewandte Chemie (International Ed. in English). 47: 2836-9. PMID 18318034 DOI: 10.1002/Anie.200705940  0.494
2008 Hwang SJ, Cho SH, Chang S. Evaluation of catalytic activity of copper salts and their removal processes in the three-component coupling reactions Pure and Applied Chemistry. 80: 873-879. DOI: 10.1351/Pac200880050873  0.509
2008 Cho SH, Hwang SJ, Chang S. Copper‐Catalyzed Three‐Component Reaction of 1‐Alkynes, Sulfonyl Azides, and Water: N‐(4‐Acetamidophenylsulfonyl)‐2‐Phenylacetamide Organic Syntheses. 85: 131-137. DOI: 10.1002/0471264229.Os085.14  0.506
2007 Cho SH, Chang S. Rate-accelerated nonconventional amide synthesis in water: a practical catalytic aldol-surrogate reaction. Angewandte Chemie (International Ed. in English). 46: 1897-900. PMID 17450617 DOI: 10.1002/Anie.200604358  0.489
2006 Chang S, Lee M, Jung DY, Yoo EJ, Cho SH, Han SK. Catalytic one-pot synthesis of cyclic amidines by virtue of tandem reactions involving intramolecular hydroamination under mild conditions. Journal of the American Chemical Society. 128: 12366-7. PMID 16984157 DOI: 10.1021/Ja064788I  0.656
2006 Yoo EJ, Bae I, Cho SH, Han H, Chang S. A facile access to N-sulfonylimidates and their synthetic utility for the transformation to amidines and amides. Organic Letters. 8: 1347-50. PMID 16562888 DOI: 10.1021/Ol060056J  0.659
2006 Bae I, Han H, Chang S, Cho SH, Yoo EJ, Cassidy MP, Raushel J, Fokin VV, Whiting M, Kellogg RM. Multicomponent reactions with ketene imine intermediates formed from the reaction of sulfonyl azides with acetylenes Chemtracts. 19: 31-37.  0.543
2005 Cho SH, Yoo EJ, Bae I, Chang S. Copper-catalyzed hydrative amide synthesis with terminal alkyne, sulfonyl azide, and water. Journal of the American Chemical Society. 127: 16046-7. PMID 16287290 DOI: 10.1021/Ja056399E  0.67
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