Shuto S - Search Results

1

A method for cleaving an allyl protecting group at the amide nitrogen of peptides by one-pot olefin isomerization-oxidation.

Kajihara K, Arisawa M, Shuto S. Kajihara K, et al. Among authors: shuto s. J Org Chem. 2008 Dec 5;73(23):9494-6. doi: 10.1021/jo801915c. J Org Chem. 2008. PMID: 18980332

2

Synthesis of the C-glycosidic analogue of adenophostin A and its uracil congener as potential IP(3) receptor ligands. Stereoselective construction of the C-glycosidic structure by a temporary silicon-tethered radical coupling reaction.

Abe H, Shuto S, Matsuda A. Abe H, et al. Among authors: shuto s. J Org Chem. 2000 Jul 14;65(14):4315-25. doi: 10.1021/jo0001333. J Org Chem. 2000. PMID: 10891132

3

Development of an efficient intermediate, alpha-[2-(trimethylsilyl)ethoxy]-2-N- [2-(trimethylsilyl)ethoxycarbonyl]folic acid, for the synthesis of folate (gamma)-conjugates, and its application to the synthesis of folate-nucleoside conjugates.

Nomura M, Shuto S, Matsuda A. Nomura M, et al. Among authors: shuto s. J Org Chem. 2000 Aug 11;65(16):5016-21. doi: 10.1021/jo000132a. J Org Chem. 2000. PMID: 10956487 No abstract available.

4

Synthesis of 3,7-anhydro-D-glycero-D-ido-octitol 1,5,6-trisphosphate as an IP(3) receptor ligand using a radical cyclization reaction with a vinylsilyl tether as the key step. Conformational restriction strategy using steric repulsion between adjacent bulky protecting groups on a pyranose ring.

Shuto S, Yahiro Y, Ichikawa S, Matsuda A. Shuto S, et al. J Org Chem. 2000 Sep 8;65(18):5547-57. doi: 10.1021/jo0002339. J Org Chem. 2000. PMID: 10970293

5

An efficient synthesis of cyclic IDP- and cyclic 8-bromo-IDP-carbocyclic-riboses using a modified Hata condensation method to form an intramolecular pyrophosphate linkage as a key step. An entry to a general method for the chemical synthesis of cyclic ADP-ribose analogues.

Fukuoka M, Shuto S, Minakawa N, Ueno Y, Matsuda A. Fukuoka M, et al. Among authors: shuto s. J Org Chem. 2000 Aug 25;65(17):5238-48. doi: 10.1021/jo0000877. J Org Chem. 2000. PMID: 10993352

6

Synthesis of pyrimidine 2'-deoxy ribonucleosides branched at the 2'-position via radical atom-transfer cyclization reaction with a vinylsilyl group as a radical-acceptor tether.

Sukeda M, Shuto S, Sugimoto I, Ichikawa S, Matsuda A. Sukeda M, et al. Among authors: shuto s. J Org Chem. 2000 Dec 29;65(26):8988-96. doi: 10.1021/jo000967l. J Org Chem. 2000. PMID: 11149841

7

Nucleosides and Nucleotides. 151. Conversion of (Z)-2'-(Cyanomethylene)-2'-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions(1).

Hassan AE, Nishizono N, Minakawa N, Shuto S, Matsuda A. Hassan AE, et al. Among authors: shuto s. J Org Chem. 1996 Sep 6;61(18):6261-6267. doi: 10.1021/jo960577s. J Org Chem. 1996. PMID: 11667465

8

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).

Hassan AE, Shuto S, Matsuda A. Hassan AE, et al. Among authors: shuto s. J Org Chem. 1997 Jan 10;62(1):11-17. doi: 10.1021/jo9613601. J Org Chem. 1997. PMID: 11671359

9

Stereo- and Regioselective Introduction of 1- or 2-Hydroxyethyl Group via Intramolecular Radical Cyclization Reaction with a Novel Silicon-Containing Tether. An Efficient Synthesis of 4'alpha-Branched 2'-Deoxyadenosines(1).

Shuto S, Kanazaki M, Ichikawa S, Minakawa N, Matsuda A. Shuto S, et al. J Org Chem. 1998 Feb 6;63(3):746-754. doi: 10.1021/jo971703a. J Org Chem. 1998. PMID: 11672069

10

Development of versatile cis- and trans-dicarbon-substituted chiral cyclopropane units: synthesis of (1S,2R)- and (1R,2R)-2-aminomethyl-1-(1H-imidazol-4-yl)cyclopropanes and their enantiomers as conformationally restricted analogues of histamine.

Kazuta Y, Matsuda A, Shuto S. Kazuta Y, et al. Among authors: shuto s. J Org Chem. 2002 Mar 8;67(5):1669-77. doi: 10.1021/jo010852x. J Org Chem. 2002. PMID: 11871901

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