Synthesis of α‑l‑Threose Nucleoside Phosphonates via Regioselective Sugar Protection von Dumbre, Shrinivas G, Jang, Mi-Yeon, Herdewijn, Piet

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Regioselective 2′-O-debenzoylation of 2',3'-di-O-benzoyl threose nucleosides von Jang, Mi-Yeon, Froeyen, Matheus, Herdewijn, Piet

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Discovery of a Potent, Orally Bioavailable PI4KIIIβ Inhibitor (UCB9608) Able To Significantly Prolong Allogeneic Organ Engraftment in Vivo von Reuberson, James, Horsley, Helen, Franklin, Richard J, Ford, Daniel, Neuss, Judi, Brookings, Daniel, Huang, Qiuya, Vanderhoydonck, Bart, Gao, Ling-Jie, Jang, Mi-Yeon, Herdewijn, Piet, Ghawalkar, Anant, Fallah-Arani, Farnaz, Khan, Adnan R, Henshall, Jamie, Jairaj, Mark, Malcolm, Sarah, Ward, Eleanor, Shuttleworth, Lindsay, Lin, Yuan, Li, Shengqiao, Louat, Thierry, Waer, Mark, Herman, Jean, Payne, Andrew, Ceska, Tom, Doyle, Carl, Pitt, Will, Calmiano, Mark, Augustin, Martin, Steinbacher, Stefan, Lammens, Alfred, Allen, Rodger

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Development of Synthetic Strategies for the Construction of Pyrido[4,3-d]pyrimidine Libraries - the Discovery of a New Class of PDE-4 Inhibitors von Jang, Mi-Yeon, De Jonghe, Steven, Gao, Ling-Jie, Rozenski, Jef, Herdewijn, Piet

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Synthesis of novel 5-amino-thiazolo[4,5-d]pyrimidines as E. coli and S. aureus SecA inhibitors von Jang, Mi-Yeon, Jonghe, Steven De, Segers, Kenneth, Anné, Jozef, Herdewijn, Piet

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Regioselective cross-coupling reactions and nucleophilic aromatic substitutions on a 5,7-dichloropyrido[4,3- d]pyrimidine scaffold von Jang, Mi-Yeon, Jonghe, Steven De, Gao, Ling-Jie, Herdewijn, Piet

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Discovery of 7-N-Piperazinylthiazolo[5,4-d]pyrimidine Analogues as a Novel Class of Immunosuppressive Agents with in Vivo Biological Activity von Jang, Mi-Yeon, Lin, Yuan, De Jonghe, Steven, Gao, Ling-Jie, Vanderhoydonck, Bart, Froeyen, Mathy, Rozenski, Jef, Herman, Jean, Louat, Thierry, Van Belle, Kristien, Waer, Mark, Herdewijn, Piet

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Synthesis, immunosuppressive activity and structure–activity relationship study of a new series of 4- N-piperazinyl-thieno[2,3- d]pyrimidine analogues von Jang, Mi-Yeon, Jonghe, Steven De, Belle, Kristien Van, Louat, Thierry, Waer, Mark, Herdewijn, Piet

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Impact of sulfur substitution on biotin binding affinity to streptavidin von Groaz, Elisabetta, Modranka, Jakub, Ploschik, Damian, Jabgunde, Amit, Froeyen, Mathy, Jang, Mi-Yeon, Wagenknecht, Hans-Achim, Herdewijn, Piet

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Impact of sulfur substitution on biotin binding affinity to streptavidin von Groaz, Elisabetta, Modranka, Jakub, Ploschik, Damian, Jabgunde, Amit, Froeyen, Mathy, Jang, Mi-Yeon, Wagenknecht, Hans-Achim, Herdewijn, Piet

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A Synthetic Substrate of DNA Polymerase Deviating from the Bases, Sugar, and Leaving Group of Canonical Deoxynucleoside Triphosphates von Jang, Mi-Yeon, Song, Xiao-Ping, Froeyen, Mathy, Marlière, Philippe, Lescrinier, Eveline, Rozenski, Jef, Herdewijn, Piet

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Toxic effects of 12 pesticides on green lacewing, Chrysoperla nipponensis (Okamoto) (Neuroptera: Chrysopidae) von Ham, Eun Hye, Lee, Jun Seok, Jang, Mi Yeon, Park, Jong Kyun

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Abstract C075: A first-in-class and highly selective SHP1 allosteric inhibitor exhibits robust anti-tumor immunity and synergizes with PD-1 blockade von Kim, Jun Gyu, Ryu, Ki Moon, Jang, Mi Yeon, Cho, Jongho, Kim, Dajeong, Seong, Dae Hyeon, Kim, Kyu Hwan, Jang, Ik-Soo, Shin, Jeong Yoon, Han, Hong Sik, Hwang, Joon Yonug, Lee, Dae Young, Ryu, Chae Lim, Lee, Song Yi, Han, Tae-Dong, Yang, SeungMin, Doh, Hyounmie

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Discovery of a Potent, Orally Bioavailable PI4KIIIβ Inhibitor (UCB9608) Able To Significantly Prolong Allogeneic Organ Engraftment in Vivo von Reuberson, James, Horsley, Helen, Franklin, Richard J, Ford, Daniel, Neuss, Judi, Brookings, Daniel, Huang, Qiuya, Vanderhoydonck, Bart, Gao, Ling-Jie, Jang, Mi-Yeon, Herdewijn, Piet, Ghawalkar, Anant, Fallah-Arani, Farnaz, Khan, Adnan R, Henshall, Jamie, Jairaj, Mark, Malcolm, Sarah, Ward, Eleanor, Shuttleworth, Lindsay, Lin, Yuan, Li, Shengqiao, Louat, Thierry, Waer, Mark, Herman, Jean, Payne, Andrew, Ceska, Tom, Doyle, Carl, Pitt, Will, Calmiano, Mark, Augustin, Martin, Steinbacher, Stefan, Lammens, Alfred, Allen, Rodger

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ChemInform Abstract: Regioselective 2′-O-Debenzoylation of 2′,3′-Di-O-benzoyl Threose Nucleosides von Jang, Mi-Yeon, Froeyen, Matheus, Herdewijn, Piet

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Synthesis of novel 5-amino-thiazolo[4,5-d]pyrimidines as E. coli and S. aureus SecA inhibitors von Jang, Mi-Yeon, De Jonghe, Steven, Segers, Kenneth, Anné, Jozef, Herdewijn, Piet

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Studies on the Total Synthesis of Amphidinolide O (II): A Stereoselective Synthesis of C1-C11 Fragment von Jang, Mi-Yeon, Kim, Jong-Woo, Lee, Duck-Hyung

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Discovery of 7-N-Piperazinylthiazolo[5,4-d]pyrimidine Analogues as a Novel Class of Immunosuppressive Agents with in Vivo Biological Activity von Jang, Mi-Yeon, Lin, Yuan, De Jonghe, Steven, Gao, Ling-Jie, Vanderhoydonck, Bart, Froeyen, Mathy, Rozenski, Jef, Herman, Jean, Louat, Thierry, Van Belle, Kristien, Waer, Mark, Herdewijn, Piet

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Regioselective Cross-Coupling Reactions and Nucleophilic Aromatic Substitutions on a 5,7-Dichloropyrido[4,3-d]pyrimidine Scaffold von Jang, Mi-Yeon, De Jonghe, Steven, Gao, Ling-Jie, Herdewijn, Piet

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Development of Synthetic Strategies for the Construction of Pyrido[4,3-d]pyrimidine Libraries - The Discovery of a New Class of PDE-4 Inhibitors von Jang, Mi-Yeon, De Jonghe, Steven, Gao, Ling-Jie, Rozenski, Jef, Herdewijn, Piet

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