Green and sustainable chemical synthesis using flow microreactors J Yoshida, H Kim, A Nagaki ChemSusChem 4 (3), 331-340, 2011 | 464 | 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 | 288 | 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 | 241 | 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 | 191 | 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 | 171 | 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 | 150 | 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 | 118 | 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 | 114 | 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 | 99 | 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 | 46 | 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 | 32 | 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 | 28 | 2017 |
Microfluidics‐Assisted Synthesis of Hierarchical Cu2O Nanocrystal as C2‐Selective CO2 Reduction Electrocatalyst M Jun, C Kwak, SY Lee, J Joo, JM Kim, DJ Im, MK Cho, H Baik, YJ Hwang, ... Small Methods 6 (5), 2200074, 2022 | 26 | 2022 |
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 |
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 | 25 | 2014 |
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 |