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Satoshi Shuto

Showing results (11-20 of 182) with videos related to

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Bioorganic & Medicinal Chemistry|May 9, 2003
Synthesis of the cyclic and acyclic acetal derivatives of 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine, a potent antitumor nucleoside. Design of prodrugs to be selectively activated in tumor tissues via the bio-reduction-hydrolysis mechanismMakoto Nomura, Satoshi Shuto, Akira Matsuda
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 21, 2017
From Peptides to Peptidomimetics: A Strategy Based on the Structural Features of CyclopropaneAkira Mizuno, Kouhei Matsui, Satoshi Shuto
The Journal of Organic Chemistry|November 5, 2008
A method for cleaving an allyl protecting group at the amide nitrogen of peptides by one-pot olefin isomerization-oxidationKouki Kajihara, Mitsuhiro Arisawa, Satoshi Shuto
The Journal of Organic Chemistry|January 10, 1997
Nucleosides and Nucleotides. 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2'-Position of 2'-[(Alkoxycarbonyl)methylene]-2'-deoxyuridines: Conversion of (Z)-2'-[(Alkoxycarbonyl)methylene]-2'-deoxyuridines into Their (E)-Isomers(1)Abdalla E. A. Hassan, Satoshi Shuto, Akira Matsuda
Nucleosides, Nucleotides & Nucleic Acids|June 13, 2019
Synthesis of 1,1,2-trisubstituted cyclopropane nucleosides in enantiomerically pure formsDaichi Fushihara, Hayato Fukuda, Hiroshi Abe, et al.
Nucleosides, Nucleotides & Nucleic Acids|October 27, 2005
Synthesis and biological activity of cyclic ADP-carbocyclic-ribose analogs: structure-activity relationship and conformational analysis of N-1-carbocyclic-ribose moietyTakashi Kudoh, Masayoshi Fukuoka, Satoshi Shuto, et al.
The Journal of Organic Chemistry|April 26, 2003
The first radical method for the introduction of an ethynyl group using a silicon tether and its application to the synthesis of 2'-deoxy-2'-C-ethynylnucleosidesMakoto Sukeda, Satoshi Ichikawa, Akira Matsuda, et al.
Organic Letters|December 15, 2015
Pd(II)-Catalyzed Alkylation of Tertiary Carbon via Directing-Group-Mediated C(sp(3))-H Activation: Synthesis of Chiral 1,1,2-Trialkyl Substituted CyclopropanesNaoyuki Hoshiya, Kei Takenaka, Satoshi Shuto, et al.
The Journal of Organic Chemistry|October 26, 2002
A highly stereoselective samarium diiodide-promoted aldol reaction with 1'-phenylseleno-2'-keto nucleosides. Synthesis of 1'alpha-branched uridine derivativesTetsuya Kodama, Satoshi Shuto, Satoshi Ichikawa, et al.
Angewandte Chemie (International Ed. in English)|March 5, 2003
Control of alpha/beta stereoselectivity in Lewis acid promoted C-glycosidations using a controlling anomeric effect based on the conformational restriction strategySatoru Tamura, Hiroshi Abe, Akira Matsuda, et al.
Pageof 19

Showing results (11-20 of 182) with videos related to

Sort By:
Pageof 19
Bioorganic & Medicinal Chemistry|May 9, 2003
Synthesis of the cyclic and acyclic acetal derivatives of 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine, a potent antitumor nucleoside. Design of prodrugs to be selectively activated in tumor tissues via the bio-reduction-hydrolysis mechanismMakoto Nomura, Satoshi Shuto, Akira Matsuda
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 21, 2017
From Peptides to Peptidomimetics: A Strategy Based on the Structural Features of CyclopropaneAkira Mizuno, Kouhei Matsui, Satoshi Shuto
The Journal of Organic Chemistry|November 5, 2008
A method for cleaving an allyl protecting group at the amide nitrogen of peptides by one-pot olefin isomerization-oxidationKouki Kajihara, Mitsuhiro Arisawa, Satoshi Shuto
The Journal of Organic Chemistry|January 10, 1997
Nucleosides and Nucleotides. 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2'-Position of 2'-[(Alkoxycarbonyl)methylene]-2'-deoxyuridines: Conversion of (Z)-2'-[(Alkoxycarbonyl)methylene]-2'-deoxyuridines into Their (E)-Isomers(1)Abdalla E. A. Hassan, Satoshi Shuto, Akira Matsuda
Nucleosides, Nucleotides & Nucleic Acids|June 13, 2019
Synthesis of 1,1,2-trisubstituted cyclopropane nucleosides in enantiomerically pure formsDaichi Fushihara, Hayato Fukuda, Hiroshi Abe, et al.
Nucleosides, Nucleotides & Nucleic Acids|October 27, 2005
Synthesis and biological activity of cyclic ADP-carbocyclic-ribose analogs: structure-activity relationship and conformational analysis of N-1-carbocyclic-ribose moietyTakashi Kudoh, Masayoshi Fukuoka, Satoshi Shuto, et al.
The Journal of Organic Chemistry|April 26, 2003
The first radical method for the introduction of an ethynyl group using a silicon tether and its application to the synthesis of 2'-deoxy-2'-C-ethynylnucleosidesMakoto Sukeda, Satoshi Ichikawa, Akira Matsuda, et al.
Organic Letters|December 15, 2015
Pd(II)-Catalyzed Alkylation of Tertiary Carbon via Directing-Group-Mediated C(sp(3))-H Activation: Synthesis of Chiral 1,1,2-Trialkyl Substituted CyclopropanesNaoyuki Hoshiya, Kei Takenaka, Satoshi Shuto, et al.
The Journal of Organic Chemistry|October 26, 2002
A highly stereoselective samarium diiodide-promoted aldol reaction with 1'-phenylseleno-2'-keto nucleosides. Synthesis of 1'alpha-branched uridine derivativesTetsuya Kodama, Satoshi Shuto, Satoshi Ichikawa, et al.
Angewandte Chemie (International Ed. in English)|March 5, 2003
Control of alpha/beta stereoselectivity in Lewis acid promoted C-glycosidations using a controlling anomeric effect based on the conformational restriction strategySatoru Tamura, Hiroshi Abe, Akira Matsuda, et al.
Pageof 19