A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents von Qin, Tian, Cornella, Josep, Li, Chao, Malins, Lara R., Edwards, Jacob T., Kawamura, Shuhei, Maxwell, Brad D., Eastgate, Martin D., Baran, Phil S.

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Practical Ni-Catalyzed Aryl–Alkyl Cross-Coupling of Secondary Redox-Active Esters von Cornella, Josep, Edwards, Jacob T, Qin, Tian, Kawamura, Shuhei, Wang, Jie, Pan, Chung-Mao, Gianatassio, Ryan, Schmidt, Michael, Eastgate, Martin D, Baran, Phil S

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Influence of a plasma-treated nutrient solution containing 2,4-dichlorobenzoic acid on the growth of cucumber in a hydroponic system von Takahashi, Katsuyuki, Kawamura, Shuhei, Takada, Ryosuke, Takaki, Koichi, Satta, Naoya, Fujio, Takuya

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Simple Sulfinate Synthesis Enables CH Trifluoromethylcyclopropanation von Gianatassio, Ryan, Kawamura, Shuhei, Eprile, Cecil L, Foo, Klement, Ge, Jason, Burns, Aaron C., Collins, Michael R., Baran, Phil S.

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Recent Developments on Modeling for a 3-DOF Micro-Hand Based on AI Methods von Kawamura, Shuhei, Deng, Mingcong

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Operator-Based Nonlinear Control for a Miniature Flexible Actuator Using the Funnel Control Method von Ueno, Keisuke, Kawamura, Shuhei, Deng, Mingcong

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Structurally Novel Highly Potent Proteasome Inhibitors Created by the Structure-Based Hybridization of Nonpeptidic Belactosin Derivatives and Peptide Boronates von Kawamura, Shuhei, Unno, Yuka, Asai, Akira, Arisawa, Mitsuhiro, Shuto, Satoshi

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Potent Proteasome Inhibitors Derived from the Unnatural cis-Cyclopropane Isomer of Belactosin A: Synthesis, Biological Activity, and Mode of Action von Kawamura, Shuhei, Unno, Yuka, List, Anja, Mizuno, Akirai, Tanaka, Motohiro, Sasaki, Takuma, Arisawa, Mitsuhiro, Asai, Akira, Groll, Michael, Shuto, Satoshi

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Modeling and System Integration for a Thin Pneumatic Rubber 3-DOF Actuator von Kawamura, Shuhei, Sudani, Mizuki, Deng, Mingcong, Noge, Yuichi, Wakimoto, Shuichi

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Investigation of the Noncovalent Binding Mode of Covalent Proteasome Inhibitors around the Transition State by Combined Use of Cyclopropylic Strain-Based Conformational Restriction... von Kawamura, Shuhei, Unno, Yuka, Tanaka, Motohiro, Sasaki, Takuma, Yamano, Akihito, Hirokawa, Takatsugu, Kameda, Tomoshi, Asai, Akira, Arisawa, Mitsuhiro, Shuto, Satoshi

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Cyclopropane-based conformational restriction of GABA by a stereochemical diversity-oriented strategy: Identification of an efficient lead for potent inhibitors of GABA transports von Nakada, Kazuaki, Yoshikawa, Mamie, Ide, Soichiro, Suemasa, Akihiro, Kawamura, Shuhei, Kobayashi, Takaaki, Masuda, Eiji, Ito, Yoshihiko, Hayakawa, Wataru, Katayama, Takahiro, Yamada, Shizuo, Arisawa, Mitsuhiro, Minami, Masabumi, Shuto, Satoshi

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Nineteen-step total synthesis of (+)-phorbol von Kawamura, Shuhei, Chu, Hang, Felding, Jakob, Baran, Phil S.

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Synthesis and pharmacological evaluation of nucleoside prodrugs designed to target siderophore biosynthesis in Mycobacterium tuberculosis von Dawadi, Surendra, Kawamura, Shuhei, Rubenstein, Anja, Remmel, Rory, Aldrich, Courtney C.

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Design and synthesis of unprecedented 9- and 10-membered cyclonucleosides with PRMT5 inhibitory activity von Kawamura, Shuhei, Palte, Rachel L., Kim, Hai-Young, Saurí, Josep, Sondey, Christopher, Mansueto, My S., Altman, Michael D., Machacek, Michelle R.

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Ligand–Phospholipid Conjugation: A Versatile Strategy for Developing Long-Acting Ligands That Bind to Membrane Proteins by Restricting the Subcellular Localization of the Ligand von Kawamura, Shuhei, Ito, Yoshihiko, Hirokawa, Takatsugu, Hikiyama, Eriko, Yamada, Shizuo, Shuto, Satoshi

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Simple Sulfinate Synthesis Enables CH Trifluoromethylcyclopropanation von Gianatassio, Ryan, Kawamura, Shuhei, Eprile, Cecil L, Foo, Klement, Ge, Jason, Burns, Aaron C., Collins, Michael R., Baran, Phil S.

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Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structure von Kawamura, Shuhei, Unno, Yuka, Asai, Akira, Arisawa, Mitsuhiro, Shuto, Satoshi

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Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketones von Kawamura, Shuhei, Unno, Yuka, Asai, Akira, Arisawa, Mitsuhiro, Shuto, Satoshi

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Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin A von Kawamura, Shuhei, Unno, Yuka, Hirokawa, Takatsugu, Asai, Akira, Arisawa, Mitsuhiro, Shuto, Satoshi

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The Discovery of Two Novel Classes of 5,5-Bicyclic Nucleoside-Derived PRMT5 Inhibitors for the Treatment of Cancer von Quiroz, Ryan V, Reutershan, Michael H, Schneider, Sebastian E, Sloman, David, Lacey, Brian M, Swalm, Brooke M, Yeung, Charles S, Gibeau, Craig, Spellman, Daniel S, Rankic, Danica A, Chen, Dapeng, Witter, David, Linn, Doug, Munsell, Erik, Feng, Guo, Xu, Haiyan, Hughes, Jonathan M. E, Lim, Jongwon, Saurí, Josep, Geddes, Kristin, Wan, Murray, Mansueto, My Sam, Follmer, Nicole E, Fier, Patrick S, Siliphaivanh, Phieng, Daublain, Pierre, Palte, Rachel L, Hayes, Robert P, Lee, Sandra, Kawamura, Shuhei, Silverman, Steven, Sanyal, Sulagna, Henderson, Timothy J, Ye, Yingchun, Gao, Yuanwei, Nicholson, Benjamin, Machacek, Michelle R

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