Year |
Citation |
Score |
2023 |
Koo B, Kim C. Synthesis of Stereocontrolled Degradable Polymer by Living Cascade Enyne Metathesis Polymerization. Angewandte Chemie (International Ed. in English). e202312399. PMID 37737689 DOI: 10.1002/anie.202312399 |
0.376 |
|
2022 |
Kim D, Yoo H, Kim K, Kim D, Kim KT, Kim C, Kim JY, Moon HR, Kim M. Post-synthetic ligand cyclization in metal-organic frameworks through functional group connection with regioisomerism. Chemical Communications (Cambridge, England). PMID 35415736 DOI: 10.1039/d2cc01031c |
0.211 |
|
2021 |
Koo B, Yoo H, Choi HJ, Kim M, Kim C, Kim KT. Visible Light Photochemical Reactions for Nucleic Acid-Based Technologies. Molecules (Basel, Switzerland). 26. PMID 33494512 DOI: 10.3390/molecules26030556 |
0.16 |
|
2020 |
Kulow RW, Wu JW, Kim C, Michaudel Q. Synthesis of unsymmetrical sulfamides and polysulfamides SuFEx click chemistry. Chemical Science. 11: 7807-7812. PMID 34094153 DOI: 10.1039/d0sc03606d |
0.581 |
|
2020 |
Hsu TW, Kim C, Michaudel Q. Stereoretentive Ring-Opening Metathesis Polymerization to Access All-cis Poly(p-phenylene vinylene)s with Living Characteristics. Journal of the American Chemical Society. PMID 32588629 DOI: 10.1021/Jacs.0C04068 |
0.724 |
|
2020 |
Lee H, Kim D, You A, Park MH, Kim M, Kim C. Transition Metal-Catalyzed α-Position Carbon–Carbon Bond Formations of Carbonyl Derivatives Catalysts. 10: 861. DOI: 10.3390/Catal10080861 |
0.311 |
|
2020 |
Kulow RW, Wu JW, Kim C, Michaudel Q. Synthesis of unsymmetrical sulfamides and polysulfamides via SuFEx click chemistry Chemical Science. 11: 7807-7812. DOI: 10.1039/D0Sc03606D |
0.635 |
|
2019 |
Yoo K, Jwa DG, Lee H, Kim HJ, Kim C, Kim M. Recent Organic Transformations with Silver Carbonate as a Key External Base and Oxidant Catalysts. 9: 1032. DOI: 10.3390/Catal9121032 |
0.402 |
|
2018 |
Kim C, Chung H. Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction. Journal of Visualized Experiments : Jove. PMID 30199020 DOI: 10.3791/58067 |
0.707 |
|
2018 |
Kim C, Chung H. Oligo(Ethylene Glycol) Length Effect of Water-Soluble Ru-Based Olefin Metathesis Catalysts on Reactivity and Removability. The Journal of Organic Chemistry. PMID 30092137 DOI: 10.1021/Acs.Joc.8B01312 |
0.704 |
|
2018 |
Kim C, Ondrusek BA, Chung H. Removable Water-Soluble Olefin Metathesis Catalyst via Host-Guest Interaction. Organic Letters. PMID 29350047 DOI: 10.1021/Acs.Orglett.7B03871 |
0.692 |
|
2018 |
Pramudya I, Kim C, Chung H. Synthesis and adhesion control of glucose-based bioadhesive via strain-promoted azide–alkyne cycloaddition Polymer Chemistry. 9: 3638-3650. DOI: 10.1039/C8Py00339D |
0.668 |
|
2014 |
Kim C, Kang S, Rhee YH. Synthesis of the tricyclic core in stemonamine alkaloids via one-pot gold(I)-catalyzed cyclization and schmidt rearrangement: formal synthesis of (±)-stemonamine. The Journal of Organic Chemistry. 79: 11119-24. PMID 25322172 DOI: 10.1021/Jo502103P |
0.6 |
|
2013 |
Park SR, Kim C, Kim DG, Thrimurtulu N, Yeom HS, Jun J, Shin S, Rhee YH. Entry to β-alkoxyacrylates via gold-catalyzed intermolecular coupling of alkynoates and allylic ethers. Organic Letters. 15: 1166-9. PMID 23444917 DOI: 10.1021/Ol4001087 |
0.602 |
|
2011 |
Lee JH, Kim C, Rhee YH. A new approach toward azabicyclic frameworks using gold(I)-catalyzed cycloisomerization of mixed N,O-Acetals of homopropargylic amines Bulletin of the Korean Chemical Society. 32: 2867-2868. DOI: 10.5012/Bkcs.2011.32.8.2867 |
0.604 |
|
2010 |
Kim C, Lim W, Rhee YH. Gold(I)-catalyzed cycloisomerization of the mixed wys-acetals generated from homopropargylic amines; mechanistic implication for the formal alkyne prins reaction Bulletin of the Korean Chemical Society. 31: 1465-1466. DOI: 10.5012/Bkcs.2010.31.6.1465 |
0.633 |
|
2009 |
Kim C, Bae HJ, Lee JH, Jeong W, Kim H, Sampath V, Rhee YH. Formal alkyne aza-prins cyclization: gold(I)-catalyzed cycloisomerization of mixed N,O-acetals generated from homopropargylic amines to highly substituted piperidines. Journal of the American Chemical Society. 131: 14660-1. PMID 19785427 DOI: 10.1021/Ja906744R |
0.618 |
|
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