| Year |
Citation |
Score |
| 2019 |
Lee JH, Choi S, Hong KB. Alkene Difunctionalization Using Hypervalent Iodine Reagents: Progress and Developments in the Past Ten Years. Molecules (Basel, Switzerland). 24. PMID 31331092 DOI: 10.3390/Molecules24142634 |
0.356 |
|
| 2018 |
Park SW, Kim SH, Song J, Park GY, Kim D, Nam TG, Hong KB. Hypervalent iodine-mediated Ritter-type amidation of terminal alkenes: The synthesis of isoxazoline and pyrazoline cores. Beilstein Journal of Organic Chemistry. 14: 1028-1033. PMID 29977375 DOI: 10.3762/Bjoc.14.89 |
0.478 |
|
| 2017 |
Yum EK, Hong KB. Synthesis of pyrrolo-heterocycles via Pd-loaded zeolite catalyzed annulation of o - haloaromatic amine with terminal alkynes Tetrahedron. 73: 6581-6586. DOI: 10.1016/J.Tet.2017.10.002 |
0.301 |
|
| 2017 |
Jeon H, Kim D, Lee JH, Song J, Lee WS, Kang DW, Kang S, Lee SB, Choi S, Hong KB. Hypervalent Iodine-Mediated Alkene Functionalization: Oxazoline and Thiazoline Synthesis via Inter-/Intramolecular Aminohydroxylation and Thioamination Advanced Synthesis & Catalysis. 360: 779-783. DOI: 10.1002/Adsc.201701087 |
0.382 |
|
| 2016 |
Kim B, Park H, Lee SK, Park SJ, Koo TS, Kang NS, Hong KB, Choi S. Systemic optimization and structural evaluation of quinoline derivatives as transthyretin amyloidogenesis inhibitors. European Journal of Medicinal Chemistry. 123: 777-787. PMID 27541261 DOI: 10.1016/J.Ejmech.2016.08.003 |
0.343 |
|
| 2015 |
Danneman MW, Hong KB, Johnston JN. A Unified Approach to the Four Azaindoline Families by Inter-/Intramolecular Annulative Diamination of Vinylpyridines. Organic Letters. 17: 3806-9. PMID 26186041 DOI: 10.1021/Acs.Orglett.5B01783 |
0.702 |
|
| 2015 |
Danneman MW, Hong KB, Johnston JN. Oxidative inter-/intermolecular alkene diamination of hydroxy styrenes with electron-rich amines. Organic Letters. 17: 2558-61. PMID 25942322 DOI: 10.1021/Acs.Orglett.5B01177 |
0.677 |
|
| 2014 |
Hong KB, Johnston JN. Alkene diamination using electron-rich amines: hypervalent iodine-promoted inter-/intramolecular C-N bond formation. Organic Letters. 16: 3804-7. PMID 24981419 DOI: 10.1021/Ol501693J |
0.695 |
|
| 2013 |
LaPorte M, Hong KB, Xu J, Wipf P. 5-Hydroxyindoles by intramolecular alkynol-furan diels-alder cycloaddition. The Journal of Organic Chemistry. 78: 167-74. PMID 23136970 DOI: 10.1021/Jo3022605 |
0.306 |
|
| 2011 |
Troyer TL, Muchalski H, Hong KB, Johnston JN. Origins of selectivity in Brønsted acid-promoted diazoalkane-azomethine reactions (the aza-Darzens aziridine synthesis). Organic Letters. 13: 1790-2. PMID 21366339 DOI: 10.1021/Ol200313M |
0.616 |
|
| 2010 |
Muchalski H, Hong KB, Johnston JN. Brønsted acid-promoted azide-olefin [3 + 2] cycloadditions for the preparation of contiguous aminopolyols: The importance of disiloxane ring size to a diastereoselective, bidirectional approach to zwittermicin A. Beilstein Journal of Organic Chemistry. 6: 1206-10. PMID 21283562 DOI: 10.3762/Bjoc.6.138 |
0.719 |
|
| 2009 |
Donahue MG, Hong KB, Johnston JN. Use of comparative triazolinium triflate fragmentation rates as a tool to assay relative competency of Brønsted bases in N-->N proton transfer. Bioorganic & Medicinal Chemistry Letters. 19: 4971-3. PMID 19640710 DOI: 10.1016/J.Bmcl.2009.07.067 |
0.723 |
|
| 2008 |
Hong KB, Donahue MG, Johnston JN. On the nature of rate acceleration in the synthesis and fragmentation of triazolines by Brønsted acid: secondary catalysis by water (hydronium triflate). Journal of the American Chemical Society. 130: 2323-8. PMID 18217758 DOI: 10.1021/Ja0779452 |
0.726 |
|
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