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 *

205 related articles for article (PubMed ID: 25005002)

  • 1. Understanding the domino retro [3+2] cycloaddition/cyclization reaction of bicyclic isoxazolidines in the synthesis of spirocyclic alkaloids. A DFT study.
    Layeb H; Nacereddine AK; Djerourou A; Domingo LR
    J Mol Model; 2014 Jul; 20(7):2347. PubMed ID: 25005002
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Highly trans-stereoselective synthesis of bicyclic isoxazolidines via copper-catalyzed triple cascade catalysis.
    Chen H; Wang Z; Zhang Y; Huang Y
    J Org Chem; 2013 Apr; 78(7):3503-9. PubMed ID: 23496240
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diastereoselective ruthenium porphyrin-catalyzed tandem nitrone formation/1,3-dipolar cycloaddition for isoxazolidines. Synthesis, in silico docking study and in vitro biological activities.
    Reddy AR; Guo Z; Siu FM; Lok CN; Liu F; Yeung KC; Zhou CY; Che CM
    Org Biomol Chem; 2012 Dec; 10(46):9165-74. PubMed ID: 22964756
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Investigation of conjugate addition/intramolecular nitrone dipolar cycloadditions and their use in the synthesis of dendrobatid alkaloid precursors.
    Horsley HT; Holmes AB; Davies JE; Goodman JM; Silva MA; Pascu SI; Collins I
    Org Biomol Chem; 2004 Apr; 2(8):1258-65. PubMed ID: 15064806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Visible-light photoredox-catalyzed synthesis of nitrones: unexpected rate acceleration by water in the synthesis of isoxazolidines.
    Hou H; Zhu S; Pan F; Rueping M
    Org Lett; 2014 Jun; 16(11):2872-5. PubMed ID: 24810928
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Intramolecular nitrone dipolar cycloadditions: control of regioselectivity and synthesis of naturally-occurring spirocyclic alkaloids.
    Hodges AJ; Adams JP; Bond AD; Holmes AB; Press NJ; Roughley SD; Ryan JH; Saubern S; Smith CJ; Turnbull MD; Newton AF
    Org Biomol Chem; 2012 Dec; 10(45):8963-74. PubMed ID: 23051904
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quantum chemical studies on the mechanistic aspects of tandem sequential cycloaddition reactions of cyclooctatetraene with ester and nitrones.
    Opoku E; Tia R; Adei E
    J Mol Graph Model; 2019 Nov; 92():17-31. PubMed ID: 31302500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Intermolecular cycloaddition of N-boranonitrone with alkenes.
    Morita N; Fukui K; Irikuchi J; Sato H; Takano Y; Okamoto I; Ishibashi H; Tamura O
    J Org Chem; 2008 Sep; 73(18):7164-74. PubMed ID: 18720968
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rapid access to spirocyclic oxindole alkaloids: application of the asymmetric palladium-catalyzed [3 + 2] trimethylenemethane cycloaddition.
    Trost BM; Bringley DA; Zhang T; Cramer N
    J Am Chem Soc; 2013 Nov; 135(44):16720-35. PubMed ID: 24083654
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Iron and ruthenium Lewis acid catalyzed asymmetric 1,3-dipolar cycloaddition reactions between nitrones and enals.
    Viton F; Bernardinelli G; Kündig EP
    J Am Chem Soc; 2002 May; 124(18):4968-9. PubMed ID: 11982355
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stereocontrolled cyclic nitrone cycloaddition strategy for the synthesis of pyrrolizidine and indolizidine alkaloids.
    Brandi A; Cardona F; Cicchi S; Cordero FM; Goti A
    Chemistry; 2009 Aug; 15(32):7808-7821. PubMed ID: 19585642
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cascade oxime formation, cyclization to a nitrone, and intermolecular dipolar cycloaddition.
    Furnival RC; Saruengkhanphasit R; Holberry HE; Shewring JR; Guerrand HD; Adams H; Coldham I
    Org Biomol Chem; 2016 Nov; 14(46):10953-10962. PubMed ID: 27819376
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Highly diastereoselective 1,3-dipolar cycloadditions of chiral non-racemic nitrones to 1,2-diaza-1,3-dienes: an experimental and computational investigation.
    Majer R; Konechnaya O; Delso I; Tejero T; Attanasi OA; Santeusanio S; Merino P
    Org Biomol Chem; 2014 Nov; 12(44):8888-901. PubMed ID: 25266221
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transannular nitrone cycloaddition. A stereocontrolled entry to the spirocyclic core of pinnaic acid.
    White JD; Blakemore PR; Korf EA; Yokochi AF
    Org Lett; 2001 Feb; 3(3):413-5. PubMed ID: 11428027
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Yb(NTf2)3-catalyzed [3 + 3] cycloaddition between isatin ketonitrones and cyclopropanes to construct novel spiro[tetrahydro-1,2-oxazine]oxindoles.
    Yang HB; Shi M
    Org Biomol Chem; 2012 Oct; 10(41):8236-43. PubMed ID: 22976783
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An investigation of the Lewis acid mediated 1,3-dipolar cycloaddition between N-benzyl-C-(2-pyridyl)nitrone and allylic alcohol. Direct entry to isoxazolidinyl C-nucleosides.
    Merino P; Tejero T; Laguna M; Cerrada E; Moreno A; Lopez JA
    Org Biomol Chem; 2003 Jul; 1(13):2336-42. PubMed ID: 12945706
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spiro sugar-isoxazolidine scaffold as useful polyfunctional building block for peptidomimetics design.
    Richard M; Chapleur Y; Pellegrini-Moïse N
    Carbohydr Res; 2016 Mar; 422():24-33. PubMed ID: 26851535
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Enantioselective syntheses of various chiral multicyclic compounds with quaternary carbon stereocenters by catalytic intramolecular cycloaddition.
    Shibata T; Tahara YK; Tamura K; Endo K
    J Am Chem Soc; 2008 Mar; 130(11):3451-7. PubMed ID: 18293972
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A concise approach to the core structures of pinnaic acid and halichlorine.
    Yang SH; Clark GR; Caprio V
    Org Biomol Chem; 2009 Jul; 7(14):2981-90. PubMed ID: 19582309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regio- and stereo-selective synthesis of carbohydrate isoxazolidines by 1,3-dipolar cycloaddition of nitrones to 5,6-dideoxy-1,2-O-isopropylidene- alpha-D-xylo-hex-5-enofuranose.
    al-Timari UA; Fisera L; Goljer I; Ertl P
    Carbohydr Res; 1992 Mar; 226(1):49-56. PubMed ID: 1499022
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.