These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 31729227)

  • 1. Diastereoselective Synthesis of Arabino- and Ribo-like Nucleoside Analogues Bearing a Stereogenic C3' All-Carbon Quaternary Center.
    Lussier T; Manchoju A; Wang G; Dostie S; Foster S; Mochirian P; Prévost M; Guindon Y
    J Org Chem; 2019 Dec; 84(24):16055-16067. PubMed ID: 31729227
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Photoredox-Catalyzed Stereoselective Radical Reactions to Synthesize Nucleoside Analogues with a C2'-Stereogenic All-Carbon Quaternary Center.
    Becerril-Jiménez F; Lussier T; Leblanc L; Eymard C; Dostie S; Prévost M; Guindon Y
    J Org Chem; 2019 Nov; 84(22):14795-14804. PubMed ID: 31638391
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diastereoselective Synthesis of C2'-Fluorinated Nucleoside Analogues Using an Acyclic Approach.
    Dostie S; Prévost M; Mochirian P; Tanveer K; Andrella N; Rostami A; Tambutet G; Guindon Y
    J Org Chem; 2016 Nov; 81(22):10769-10790. PubMed ID: 27736093
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nucleotide Analogues Bearing a C2' or C3'-Stereogenic All-Carbon Quaternary Center as SARS-CoV-2 RdRp Inhibitors.
    Manchoju A; Zelli R; Wang G; Eymard C; Oo A; Nemer M; Prévost M; Kim B; Guindon Y
    Molecules; 2022 Jan; 27(2):. PubMed ID: 35056878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis of 4'-Thionucleoside Analogues Bearing a C2' Stereogenic All-Carbon Quaternary Center.
    Eymard C; Manchoju A; Almazloum A; Dostie S; Prévost M; Nemer M; Guindon Y
    Molecules; 2024 Apr; 29(7):. PubMed ID: 38611926
    [TBL] [Abstract][Full Text] [Related]  

  • 6. One-electron oxidation of gemcitabine and analogs: mechanism of formation of C3' and C2' sugar radicals.
    Adhikary A; Kumar A; Rayala R; Hindi RM; Adhikary A; Wnuk SF; Sevilla MD
    J Am Chem Soc; 2014 Nov; 136(44):15646-53. PubMed ID: 25296262
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Construction of quaternary stereocenters at carbon 2' of nucleosides.
    Liang Y; Smerznak E; Wnuk SF
    Carbohydr Res; 2023 Jun; 528():108814. PubMed ID: 37087776
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A stereoselective approach to β-L-arabino nucleoside analogues: synthesis and cyclization of acyclic 1',2'-syn N,O-acetals.
    Dostie S; Prévost M; Guindon Y
    J Org Chem; 2012 Sep; 77(17):7176-86. PubMed ID: 22873650
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Computer modeling studies of ribonuclease T1-guanosine monophosphate complexes.
    Balaji PV; Saenger W; Rao VS
    Biopolymers; 1990; 30(3-4):257-72. PubMed ID: 2177661
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Raman spectra of left-handed DNA oligomers incorporating adenine-thymine base pairs+.
    Benevides JM; Wang AH; van der Marel GA; van Boom JH; Rich A; Thomas GJ
    Nucleic Acids Res; 1984 Jul; 12(14):5913-25. PubMed ID: 6462921
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis of the first example of a C2-C3/C2'-C3'-endo unsaturated pyrrolo[2,1-c][1,4]benzodiazepine dimer.
    Gregson SJ; Howard PW; Corcoran KE; Jenkins TC; Kelland LR; Thurston DE
    Bioorg Med Chem Lett; 2001 Nov; 11(21):2859-62. PubMed ID: 11597416
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The C2'- and C3'-endo equilibrium for AMP molecules bound in the cystathionine-beta-synthase domain.
    Feng N; Qi C; Hou YJ; Zhang Y; Wang DC; Li DF
    Biochem Biophys Res Commun; 2018 Mar; 497(2):646-651. PubMed ID: 29453981
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Conformational properties of dinucleoside monophosphates in solution: dipurines and dipyrimidines.
    Lee CH; Ezra FS; Kondo NS; Sarma RH; Danyluk SS
    Biochemistry; 1976 Aug; 15(16):3627-39. PubMed ID: 952881
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Conformational flexibility in RNA: the role of dihydrouridine.
    Dalluge JJ; Hashizume T; Sopchik AE; McCloskey JA; Davis DR
    Nucleic Acids Res; 1996 Mar; 24(6):1073-9. PubMed ID: 8604341
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dual-face nucleoside scaffold featuring a stereogenic all-carbon quaternary center. Intramolecular silicon tethered group-transfer reaction.
    Tambutet G; Becerril-Jiménez F; Dostie S; Simard R; Prévost M; Mochirian P; Guindon Y
    Org Lett; 2014 Nov; 16(21):5698-701. PubMed ID: 25320862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of C3' modified nucleosides for selective generation of the C3'-deoxy-3'-thymidinyl radical: a proposed intermediate in LEE induced DNA damage.
    Audat SA; Love CT; Al-Oudat BA; Bryant-Friedrich AC
    J Org Chem; 2012 Apr; 77(8):3829-37. PubMed ID: 22468713
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diastereoselective synthesis of the indeno-tetrahydropyridine core bearing a diaryl-substituted stereogenic quaternary carbon center of haouamine B.
    Tanaka T; Inui H; Kida H; Kodama T; Okamoto T; Takeshima A; Tachi Y; Morimoto Y
    Chem Commun (Camb); 2011 Mar; 47(10):2949-51. PubMed ID: 21240443
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stereoselective Synthesis of
    Chen S; Zhang Z; Jiang C; Zhao C; Luo H; Huang J; Yang Z
    ACS Omega; 2021 Jul; 6(29):18848-18859. PubMed ID: 34337224
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural analysis of 2',3'-dideoxyinosine, 2',3'-dideoxyadenosine, 2',3'-dideoxyguanosine and 2',3'-dideoxycytidine by 500-MHz 1H-NMR spectroscopy and ab-initio molecular orbital calculations.
    Plavec J; Koole LH; Chattopadhyaya J
    J Biochem Biophys Methods; 1992 Dec; 25(4):253-72. PubMed ID: 1337354
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diastereoselective synthesis of vicinal tertiary and
    Goldfogel MJ; Meek SJ
    Chem Sci; 2016 Jul; 7(7):4079-4084. PubMed ID: 30155052
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.