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Journal Abstract Search

131 related items for PubMed ID: 8247787

  • 1. Design and synthesis of regioselective cleaving reagents for oligonucleotides.
    Mori S, Ohgo Y, Tanaka H, Katoh A, Kaji H, Samejima T, Mitsunobu O.
    Nucleic Acids Symp Ser; 1993; (29):45-6. PubMed ID: 8247787
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  • 2. Synthesis of a library of allyl alpha-L-arabinofuranosyl-alpha- or beta-D-xylopyranosides; route to higher oligomers.
    Utille JP, Jeacomine I.
    Carbohydr Res; 2007 Dec 10; 342(17):2649-56. PubMed ID: 17904112
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  • 10. D-Arabinose-based synthesis of homo-C-d4T and homo-C-thymidine.
    Doboszewski B.
    Nucleosides Nucleotides Nucleic Acids; 2009 Oct 10; 28(10):875-901. PubMed ID: 20183559
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  • 11. Picolinoxy group, a new leaving group for anti SN2' selective allylic substitution with aryl anions based on Grignard reagents.
    Kiyotsuka Y, Acharya HP, Katayama Y, Hyodo T, Kobayashi Y.
    Org Lett; 2008 May 01; 10(9):1719-22. PubMed ID: 18396885
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  • 14. Convenient synthesis of allylic thioethers from phosphorothioate esters and alcohols.
    Robertson F, Wu J.
    Org Lett; 2010 Jun 04; 12(11):2668-71. PubMed ID: 20441179
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  • 16. Design, synthesis and antiviral activity of novel 4,5-disubstituted 7-(beta-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazines and the novel 3-amino-5-methyl-1-(beta-D-ribofuranosyl)- and 3-amino-5-methyl-1-(2-deoxy-beta-D-ribofuranosyl)-1,5-dihydro-1,4,5,6,7,8-hexaazaacenaphthylene as analogues of triciribine.
    Migawa MT, Drach JC, Townsend LB.
    J Med Chem; 2005 Jun 02; 48(11):3840-51. PubMed ID: 15916436
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  • 17. Highly functionalised cyclobutanols via samarium(II) iodide-induced pinacol cyclisations of carbohydrate-derived 1,4-diketones.
    Williams DB, Caddy J, Blann K.
    Carbohydr Res; 2005 May 23; 340(7):1301-9. PubMed ID: 15854599
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  • 18. Ring opening of acylated β-d-arabinofuranose 1,2,5-orthobenzoates with nucleophiles allows access to novel selectively-protected arabinofuranose building blocks.
    Podvalnyy NM, Sedinkin SL, Abronina PI, Zinin AI, Fedina KG, Torgov VI, Kononov LO.
    Carbohydr Res; 2011 Jan 03; 346(1):7-15. PubMed ID: 21109236
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  • 19. The thio-Mitsunobu reaction: a useful tool for the preparation of 2,5-anhydro-2-thio- and 3,5-anhydro-3-thiopentofuranosides.
    Schulze O, Voss J, Adiwidjaja G, Olbrich F.
    Carbohydr Res; 2004 Jul 12; 339(10):1787-802. PubMed ID: 15220089
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  • 20. X-ray structure of 1,3,4-tri-O-acetyl-2-deoxy-beta-d-erythro-pentopyranose.
    Chen JJ, Gao JR, Han L, Jia JH, Sheng WJ, Li YJ.
    Carbohydr Res; 2009 Oct 12; 344(15):2056-9. PubMed ID: 19616773
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