| Green and sustainable chemical synthesis using flow microreactors J Yoshida, H Kim, A Nagaki ChemSusChem 4 (3), 331-340, 2011 | 458 | 2011 |
| A flow-microreactor approach to protecting-group-free synthesis using organolithium compounds H Kim, A Nagaki, J Yoshida Nature communications 2 (1), 264, 2011 | 283 | 2011 |
| Submillisecond organic synthesis: Outpacing Fries rearrangement through microfluidic rapid mixing H Kim, KI Min, K Inoue, DJ Im, DP Kim, J Yoshida Science 352 (6286), 691-694, 2016 | 236 | 2016 |
| Skeletal Octahedral Nanoframe with Cartesian Coordinates via Geometrically Precise Nanoscale Phase Segregation in a Pt@Ni Core–Shell Nanocrystal A Oh, H Baik, DS Choi, JY Cheon, B Kim, H Kim, SJ Kwon, SH Joo, ... ACS nano 9 (3), 2856-2867, 2015 | 189 | 2015 |
| Aryllithium compounds bearing alkoxycarbonyl groups: generation and reactions using a microflow system A Nagaki, H Kim, JI Yoshida Angewandte Chemie-International Edition 47 (41), 7833-7836, 2008 | 168 | 2008 |
| Nitro‐substituted aryl lithium compounds in microreactor synthesis: switch between kinetic and thermodynamic control A Nagaki, H Kim, J Yoshida Angewandte Chemie International Edition 48 (43), 8063-8065, 2009 | 147 | 2009 |
| Integrated Micro Flow Synthesis Based on Sequential Br–Li Exchange Reactions of p‐, m‐, and o‐Dibromobenzenes A Nagaki, Y Tomida, H Usutani, H Kim, N Takabayashi, T Nokami, ... Chemistry–An Asian Journal 2 (12), 1513-1523, 2007 | 117 | 2007 |
| Generation and reaction of cyano-substituted aryllithium compounds using microreactors A Nagaki, H Kim, H Usutani, C Matsuo, J Yoshida Organic & biomolecular chemistry 8 (5), 1212-1217, 2010 | 110 | 2010 |
| A flow microreactor system enables organolithium reactions without protecting alkoxycarbonyl groups A Nagaki, H Kim, Y Moriwaki, C Matsuo, J Yoshida Chemistry–A European Journal 16 (36), 11167-11177, 2010 | 96 | 2010 |
| Integrated One‐Flow Synthesis of Heterocyclic Thioquinazolinones through Serial Microreactions with Two Organolithium Intermediates H Kim, HJ Lee, DP Kim Angewandte Chemie International Edition 54 (6), 1877-1880, 2015 | 72 | 2015 |
| “Impossible” chemistries based on flow and micro J Yoshida, H Kim, A Nagaki Journal of Flow Chemistry 7 (3-4), 60-64, 2017 | 62 | 2017 |
| Synthesis of functionalized aryl fluorides using organolithium reagents in flow microreactors. A Nagaki, Y Uesugi, H Kim, J Yoshida Chemistry-An Asian Journal 8 (4), 2013 | 47 | 2013 |
| Flash synthesis of TAC-101 and its analogues from 1, 3, 5-tribromobenzene using integrated flow microreactor systems A Nagaki, K Imai, H Kim, J Yoshida RSC advances 1 (5), 758-760, 2011 | 41 | 2011 |
| A Catalyst‐Free Amination of Functional Organolithium Reagents by Flow Chemistry H Kim, Y Yonekura, J Yoshida Angewandte Chemie International Edition 57 (15), 4063-4066, 2018 | 39 | 2018 |
| From p‐Xylene to Ibuprofen in Flow: Three‐Step Synthesis by a Unified Sequence of Chemoselective C−H Metalations HJ Lee, H Kim, DP Kim Chemistry–A European Journal 25 (50), 11641-11645, 2019 | 33 | 2019 |
| Harnessing [1, 4],[1, 5], and [1, 6] Anionic Fries‐type Rearrangements by Reaction‐Time Control in Flow H Kim, K Inoue, J Yoshida Angewandte Chemie 129 (27), 7971-7974, 2017 | 26 | 2017 |
| Control of tandem isomerizations: flow-assisted reactions of o-lithiated aryl benzyl ethers HJ Lee, H Kim, J Yoshida, DP Kim Chemical communications 54 (5), 547-550, 2018 | 25 | 2018 |
| Anti-Human Rhinoviral Activity of Polybromocatechol Compounds Isolated from the Rhodophyta, Neorhodomela aculeata SH Park, JH Song, T Kim, WS Shin, GM Park, S Lee, YJ Kim, P Choi, ... Marine drugs 10 (10), 2222-2233, 2012 | 25 | 2012 |
| A monolithic and flexible fluoropolymer film microreactor for organic synthesis applications JO Kim, H Kim, DH Ko, KI Min, SY Park, DP Kim Lab on a Chip 14 (21), 4270-4276, 2014 | 24 | 2014 |
| Enhanced Controllability of Fries Rearrangements Using High‐Resolution 3D‐Printed Metal Microreactor with Circular Channel HJ Lee, RC Roberts, DJ Im, SJ Yim, H Kim, JT Kim, DP Kim Small 15 (50), 1905005, 2019 | 23 | 2019 |
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