Soon H. Hong, Ph.D.
Affiliations: | 2007 | Chemistry | California Institute of Technology, Pasadena, CA |
Area:
Organic chemistryGoogle:
"Soon Hong"Mean distance: 6.89 | S | N | B | C | P |
Parents
Sign in to add mentor| Robert Howard Grubbs | grad student | 2007 | Caltech | |
| (Improvement of Olefin Metathesis Efficiency through Understanding Catalyst Stability.) | ||||
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Publications
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| Jung K, Kim K, Sung J, et al. (2018) Toward Perfect Regiocontrol for β-Selective Cyclopolymerization Using a Ru-Based Olefin Metathesis Catalyst Macromolecules. 51: 4564-4571 |
| Kim D, Kang B, Hong SH. (2016) Ruthenium-catalyzed selective imine synthesis from nitriles and secondary alcohols under hydrogen acceptor- and base-free conditions Organic Chemistry Frontiers. 3: 475-479 |
| Kim K, Hong SH. (2015) Iridium-catalyzed single-step N-substituted lactam synthesis from lactones and amines. The Journal of Organic Chemistry. 80: 4152-6 |
| Das AK, Park S, Muthaiah S, et al. (2015) Ligand- and Acid-Free Gold(I) Chloride Catalyzed Hydration of Terminal Alkynes Synlett. 26: 2517-2520 |
| Chen C, Kim MH, Hong SH. (2015) N-heterocyclic carbene-based ruthenium-catalyzed direct amidation of aldehydes with amines Organic Chemistry Frontiers. 2: 241-247 |
| Kim K, Kang B, Hong SH. (2015) N-Heterocyclic carbene-based well-defined ruthenium hydride complexes for direct amide synthesis from alcohols and amines under base-free conditions Tetrahedron. 71: 4565-4569 |
| Song HJ, Kim JC, Lee CW, et al. (2015) Reversible Li-storage in Titanium(III) Oxide Nanosheets Electrochimica Acta. 170: 25-32 |
| Kang B, Hong SH. (2015) Hydrogen acceptor- and base-free N-formylation of nitriles and amines using methanol as C1 source Advanced Synthesis and Catalysis. 357: 834-840 |
| Kim S, Hong SH. (2015) Copper-catalyzed N-aryl-β-enaminonitrile synthesis utilizing isocyanides as the nitrogen source Advanced Synthesis and Catalysis. 357: 1004-1012 |
| Kim SM, Lee D, Hong SH. (2014) Gold(I)-catalyzed, stereocontrolled enamide synthesis from primary amides and propargyl aldehydes using a tandem strategy. Organic Letters. 16: 6168-71 |