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Journal Abstract Search

120 related items for PubMed ID: 26933954

  • 1.
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  • 2. Antiviral and Cytostatic Evaluation of 5-(1-Halo-2-sulfonylvinyl)- and 5-(2-Furyl)uracil Nucleosides.
    Wen Z, Suzol SH, Peng J, Liang Y, Snoeck R, Andrei G, Liekens S, Wnuk SF.
    Arch Pharm (Weinheim); 2017 Apr; 350(3-4):. PubMed ID: 28304114
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  • 3. An alternative method for the synthesis of 2'-halogeno-1',2'-unsaturated uridine derivatives through syn-elimination of pivalic acid of 2'-halogeno- 2'-deoxy-1'-pivaloyloxyuracil nucleoside: preparation of its 2'-C-branched nucleosides.
    Haraguchi K, Gen E, Kumamoto H, Itoh Y, Tanaka H.
    Nucleosides Nucleotides Nucleic Acids; 2020 Apr; 39(1-3):426-438. PubMed ID: 31429364
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  • 5. Synthesis and antitumor evaluation of cis-(1,2-diaminoethane) dichloroplatinum (II) complexes linked to 5- and 6-methyleneuracil and -uridine analogues.
    Kim JC, Lee MH, Choi SK.
    Arch Pharm Res; 1998 Aug; 21(4):465-9. PubMed ID: 9875477
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  • 7. Pyrimidine Nucleosides with a Reactive (β-Chlorovinyl)sulfone or (β-Keto)sulfone Group at the C5 Position, Their Reactions with Nucleophiles and Electrophiles, and Their Polymerase-Catalyzed Incorporation into DNA.
    Suzol SH, Howlader AH, Wen Z, Ren Y, Laverde EE, Garcia C, Liu Y, Wnuk SF.
    ACS Omega; 2018 Apr 30; 3(4):4276-4288. PubMed ID: 29732453
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  • 11. A new entry to the stereoselective introduction of an ethynyl group by a radical reaction: synthesis of the potential antimetabolite 2'-deoxy-2'-C-ethynyluridine.
    Sukeda M, Ichikawa S, Matsuda A, Shuto S.
    Angew Chem Int Ed Engl; 2002 Dec 16; 41(24):4748-50. PubMed ID: 12481347
    [No Abstract] [Full Text] [Related]

  • 12. Ring opening of nucleoside 1',2'-epoxides with organoaluminum reagents: stereoselective entry to ribonucleosides branched at the anomeric position.
    Haraguchi K, Kubota Y, Tanaka H.
    J Org Chem; 2004 Mar 19; 69(6):1831-6. PubMed ID: 15058925
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  • 13. Iron halide-mediated regio- and stereoselective halosulfonylation of terminal alkynes with sulfonylhydrazides: synthesis of (E)-β-chloro and bromo vinylsulfones.
    Li X, Shi X, Fang M, Xu X.
    J Org Chem; 2013 Sep 20; 78(18):9499-504. PubMed ID: 23978040
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  • 14. Halogenation of 6-O-cyclouracil nucleosides.
    Maruyama T, Honjo M.
    Nucleic Acids Symp Ser; 1980 Sep 20; (8):s45-7. PubMed ID: 7255195
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  • 15. Application of germyldesulfonylation reactions to the synthesis of germanium-containing nucleoside analogues.
    Wnuk SF, Sacasa PR, Restrepo J.
    Nucleosides Nucleotides Nucleic Acids; 2009 May 20; 28(5):537-49. PubMed ID: 20183601
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  • 16. The synthesis of some branched-chain-sugar nucleoside analogues.
    Ashwell M, Jones AS, Walker RT.
    Nucleic Acids Res; 1987 Mar 11; 15(5):2157-66. PubMed ID: 3562223
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  • 17. Organoselenium-mediated addition of carbon radicals to 4',5'-unsaturated uracil-nucleosides and its stereocontrol.
    Haraguchi K, Tanaka H, Miyasaka T.
    Nucleic Acids Symp Ser; 1989 Mar 11; (21):77-8. PubMed ID: 2608487
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  • 18. An efficient route to acyclic C-nucleosides and fused-ring analogues of uridine from exo-glycals.
    Enderlin G, Taillefumier C, Didierjean C, Chapleur Y.
    J Org Chem; 2009 Nov 06; 74(21):8388-91. PubMed ID: 19791762
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  • 19. Rhodium(I)-catalyzed addition of arylboronic acids to (benzyl-/arylsulfonyl)acetonitriles: efficient synthesis of (Z)-β-sulfonylvinylamines and β-keto sulfones.
    Tsui GC, Glenadel Q, Lau C, Lautens M.
    Org Lett; 2011 Jan 21; 13(2):208-11. PubMed ID: 21142088
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  • 20. 6-Substituted and 5,6-disubstituted derivatives of uridine: stereoselective synthesis, interaction with uridine phosphorylase, and in vitro antitumor activity.
    Felczak K, Drabikowska AK, Vilpo JA, Kulikowski T, Shugar D.
    J Med Chem; 1996 Apr 12; 39(8):1720-8. PubMed ID: 8648611
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