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Satoshi Shuto

Showing results (41-50 of 182) with videos related to

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Bioorganic & Medicinal Chemistry|May 13, 2014
Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketonesShuhei Kawamura, Yuka Unno, Akira Asai, et al.
The Journal of Organic Chemistry|June 6, 2017
Tethered 1,2-Si-Group Migrations in Radical-Mediated Ring Enlargements of Cyclic Alkoxysilanes: An EPR Spectroscopic and Computational InvestigationJohn C Walton, Ryutaro Kanada, Takeaki Iwamoto, et al.
Bioorganic & Medicinal Chemistry|September 17, 2008
Synthesis of 1-arylpiperazyl-2-phenylcyclopropanes designed as antidopaminergic agents: cyclopropane-based conformationally restricted analogs of haloperidolKazuya Yamaguchi, Yuji Kazuta, Kazufumi Hirano, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Synthesis of 5''-substituted cyclic ADP-carbocyclic-ribose as biological toolsNatsumi Sakaguchi, Takashi Kudoh, Takashi Murayama, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 24, 2016
Highly Conformationally Restricted Cyclopropane Tethers with Three-Dimensional Structural Diversity Drastically Enhance the Cell Permeability of Cyclic PeptidesKouhei Matsui, Yasuto Kido, Ryosuke Watari, et al.
Journal of Medicinal Chemistry|September 1, 2006
Stereochemical diversity-oriented conformational restriction strategy. Development of potent histamine H3 and/or H4 receptor antagonists with an imidazolylcyclopropane structureMizuki Watanabe, Yuji Kazuta, Hideki Hayashi, et al.
Organic Letters|January 18, 2019
Synthesis of Enantiomerically Pure 1,2,3-Trisubstituted Cyclopropane Nucleosides Using Pd-Catalyzed Substitution via Directing Group-Mediated C(sp<sup>3</sup>)-H Activation as a Key StepTakaaki Minami, Kohtaro Fukuda, Naoyuki Hoshiya, et al.
Organic & Biomolecular Chemistry|March 25, 2006
Synthesis of 3'-beta-carbamoylmethylcytidine (CAMC) and its derivatives as potential antitumor agentsSatoshi Ichikawa, Noriaki Minakawa, Satoshi Shuto, et al.
Journal of Medicinal Chemistry|April 14, 2018
Ligand-Phospholipid Conjugation: A Versatile Strategy for Developing Long-Acting Ligands That Bind to Membrane Proteins by Restricting the Subcellular Localization of the LigandShuhei Kawamura, Yoshihiko Ito, Takatsugu Hirokawa, et al.
Organic Letters|March 13, 2025
Highly <i>Z-</i>Selective Julia-Kocienski Olefination Using <i>N</i>-Sulfonylimines and Its Mechanistic Insights from DFT CalculationsTakuma Chizaki, Koichi Fujiwara, Junko Fujimoto, et al.
Pageof 19

Showing results (41-50 of 182) with videos related to

Sort By:
Pageof 19
Bioorganic & Medicinal Chemistry|May 13, 2014
Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketonesShuhei Kawamura, Yuka Unno, Akira Asai, et al.
The Journal of Organic Chemistry|June 6, 2017
Tethered 1,2-Si-Group Migrations in Radical-Mediated Ring Enlargements of Cyclic Alkoxysilanes: An EPR Spectroscopic and Computational InvestigationJohn C Walton, Ryutaro Kanada, Takeaki Iwamoto, et al.
Bioorganic & Medicinal Chemistry|September 17, 2008
Synthesis of 1-arylpiperazyl-2-phenylcyclopropanes designed as antidopaminergic agents: cyclopropane-based conformationally restricted analogs of haloperidolKazuya Yamaguchi, Yuji Kazuta, Kazufumi Hirano, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Synthesis of 5''-substituted cyclic ADP-carbocyclic-ribose as biological toolsNatsumi Sakaguchi, Takashi Kudoh, Takashi Murayama, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 24, 2016
Highly Conformationally Restricted Cyclopropane Tethers with Three-Dimensional Structural Diversity Drastically Enhance the Cell Permeability of Cyclic PeptidesKouhei Matsui, Yasuto Kido, Ryosuke Watari, et al.
Journal of Medicinal Chemistry|September 1, 2006
Stereochemical diversity-oriented conformational restriction strategy. Development of potent histamine H3 and/or H4 receptor antagonists with an imidazolylcyclopropane structureMizuki Watanabe, Yuji Kazuta, Hideki Hayashi, et al.
Organic Letters|January 18, 2019
Synthesis of Enantiomerically Pure 1,2,3-Trisubstituted Cyclopropane Nucleosides Using Pd-Catalyzed Substitution via Directing Group-Mediated C(sp<sup>3</sup>)-H Activation as a Key StepTakaaki Minami, Kohtaro Fukuda, Naoyuki Hoshiya, et al.
Organic & Biomolecular Chemistry|March 25, 2006
Synthesis of 3'-beta-carbamoylmethylcytidine (CAMC) and its derivatives as potential antitumor agentsSatoshi Ichikawa, Noriaki Minakawa, Satoshi Shuto, et al.
Journal of Medicinal Chemistry|April 14, 2018
Ligand-Phospholipid Conjugation: A Versatile Strategy for Developing Long-Acting Ligands That Bind to Membrane Proteins by Restricting the Subcellular Localization of the LigandShuhei Kawamura, Yoshihiko Ito, Takatsugu Hirokawa, et al.
Organic Letters|March 13, 2025
Highly <i>Z-</i>Selective Julia-Kocienski Olefination Using <i>N</i>-Sulfonylimines and Its Mechanistic Insights from DFT CalculationsTakuma Chizaki, Koichi Fujiwara, Junko Fujimoto, et al.
Pageof 19