| Year |
Citation |
Score |
| 2023 |
Kim G, Kim M, Ryu C, Choi J, Cho SH. Anion-Mediated, Stereospecific Synthesis of Secondary and Tertiary Cyclopropylboronates from Chiral Epoxides and -Diborylalkanes. Organic Letters. PMID 37227114 DOI: 10.1021/acs.orglett.3c01395 |
0.345 |
|
| 2023 |
Jung Y, Yoo SY, Jin Y, You J, Han S, Yu J, Park Y, Cho SH. Iridium-Catalyzed Chemo-, Diastereo-, and Enantioselective Allyl-Allyl Coupling: Accessing All Four Stereoisomers of (E)-1-Boryl-Substituted 1,5-Dienes by Chirality Pairing. Angewandte Chemie (International Ed. in English). e202218794. PMID 36718077 DOI: 10.1002/anie.202218794 |
0.602 |
|
| 2022 |
Han S, Lee Y, Jung Y, Cho SH. Stereoselective Access to Tetra- and Tri-Substituted Fluoro- and Chloro-borylalkenes via Boron-Wittig Reaction. Angewandte Chemie (International Ed. in English). PMID 35997761 DOI: 10.1002/anie.202210532 |
0.355 |
|
| 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 |
0.431 |
|
| 2021 |
Kim M, Park B, Shin M, Kim S, Kim J, Baik MH, Cho SH. Copper-Catalyzed Enantiotopic-Group-Selective Allylation of -Diborylalkanes. Journal of the American Chemical Society. PMID 33393768 DOI: 10.1021/jacs.0c11750 |
0.378 |
|
| 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 |
0.374 |
|
| 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 |
0.406 |
|
| 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 |
0.46 |
|
| 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 |
0.407 |
|
| 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 |
0.444 |
|
| 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 |
0.429 |
|
| 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 |
0.463 |
|
| 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 |
0.474 |
|
| 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 |
0.445 |
|
| 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 |
0.502 |
|
| 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 |
0.342 |
|
| 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 |
0.453 |
|
| 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 |
0.487 |
|
| 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 |
0.352 |
|
| 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 |
0.435 |
|
| 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 |
0.371 |
|
| 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 |
0.463 |
|
| 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 |
0.52 |
|
| 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 |
0.478 |
|
| 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 |
0.316 |
|
| 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 |
0.319 |
|
| 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 |
0.582 |
|
| 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 |
0.546 |
|
| 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 |
0.53 |
|
| 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 |
0.492 |
|
| 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 |
0.487 |
|
| 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 |
0.473 |
|
| 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 |
0.513 |
|
| 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 |
0.546 |
|
| 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 |
0.488 |
|
| 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 |
0.522 |
|
| 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 |
0.53 |
|
| 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 |
0.516 |
|
| 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 |
0.541 |
|
| 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 |
0.517 |
|
| 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 |
0.53 |
|
| 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 |
0.527 |
|
| 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 |
0.501 |
|
| 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 |
0.678 |
|
| 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 |
0.687 |
|
| 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. |
0.541 |
|
| 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 |
0.692 |
|
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