BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 23835754)

  • 1. Formation of tetrahydrofurans via a 5-endo-tet cyclization of aziridines--synthesis of (-)-pachastrissamine.
    Lin CW; Liu SW; Hou DR
    Org Biomol Chem; 2013 Aug; 11(32):5292-9. PubMed ID: 23835754
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficient synthesis of isochromanones and isoquinolines via Yb(OTf)3-catalyzed tandem oxirane/aziridine ring opening/Friedel-Crafts cyclization.
    Wei L; Zhang J
    Chem Commun (Camb); 2012 Mar; 48(20):2636-8. PubMed ID: 22294197
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans.
    Unsworth WP; Clark N; Ronson TO; Stevens K; Thompson AL; Lamont SG; Robertson J
    Chem Commun (Camb); 2014 Oct; 50(77):11393-6. PubMed ID: 25126655
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis of pachastrissamine from phytosphingosine: a comparison of cyclic sulfate vs an epoxide intermediate in cyclization.
    Lee T; Lee S; Kwak YS; Kim D; Kim S
    Org Lett; 2007 Feb; 9(3):429-32. PubMed ID: 17249779
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III).
    Vasconcelos RS; Silva LF; Giannis A
    J Org Chem; 2011 Mar; 76(5):1499-502. PubMed ID: 21244003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 5- And 6-exocyclic products, cis-2,3,5-trisubstituted tetrahydrofurans, and cis-2,3,6-trisubstituted tetrahydropyrans via Prins-type cyclization.
    Chavre SN; Choo H; Lee JK; Pae AN; Kim Y; Cho YS
    J Org Chem; 2008 Oct; 73(19):7467-71. PubMed ID: 18761436
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Highly stereoselective directed reactions and an efficient synthesis of azafuranoses from a chiral aziridine.
    Lee H; Kim JH; Lee WK; Cho J; Nam W; Lee J; Ha HJ
    Org Biomol Chem; 2013 Jun; 11(22):3629-34. PubMed ID: 23538672
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ring Opening of Aziridines by Pendant Silanols Allows for Stereospecific Preparations of 1'-Amino-tetrahydrofurans.
    Nirpal AK; Nagamalla S; Mague JT; Sathyamoorthi S
    J Org Chem; 2023 Jul; 88(13):9136-9156. PubMed ID: 37253098
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of (+)-lycoricidine by the application of oxidative and regioselective ring-opening of aziridines.
    Yadav JS; Satheesh G; Murthy CV
    Org Lett; 2010 Jun; 12(11):2544-7. PubMed ID: 20441205
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stereoselective divergent synthesis of four diastereomers of pachastrissamine (jaspine B).
    Yoshimitsu Y; Inuki S; Oishi S; Fujii N; Ohno H
    J Org Chem; 2010 Jun; 75(11):3843-6. PubMed ID: 20408556
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines.
    Kelley BT; JoulliƩ MM
    Org Lett; 2010 Oct; 12(19):4244-7. PubMed ID: 20812750
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Concise synthesis of (+)-allo-kainic acid via MgI2-mediated tandem aziridine ring opening-formal [3 + 2] cycloaddition.
    Arena G; Chen CC; Leonori D; Aggarwal VK
    Org Lett; 2013 Aug; 15(16):4250-3. PubMed ID: 23909824
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis of cis- and trans-2,5-disubstituted tetrahydrofurans by a tandem dihydroxylation-SN2 cyclization sequence.
    Marshall JA; Sabatini JJ
    Org Lett; 2005 Oct; 7(22):4819-22. PubMed ID: 16235897
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enantioselective syntheses of pachastrissamine and jaspine A via hydroxylactonization of a chiral epoxy ester.
    Urano H; Enomoto M; Kuwahara S
    Biosci Biotechnol Biochem; 2010; 74(1):152-7. PubMed ID: 20057132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ring-construction/stereoselective functionalization cascade: total synthesis of pachastrissamine (jaspine B) through palladium-catalyzed bis-cyclization of bromoallenes.
    Inuki S; Yoshimitsu Y; Oishi S; Fujii N; Ohno H
    Org Lett; 2009 Oct; 11(19):4478-81. PubMed ID: 19739618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Stereoselective synthesis of novel cyclopropyl analogues of known cysteine protease inhibitors.
    Kumar JS; Roy S; Datta A
    Bioorg Med Chem Lett; 1999 Feb; 9(4):513-4. PubMed ID: 10098652
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ring-construction/stereoselective functionalization cascade: total synthesis of pachastrissamine (jaspine B) through palladium-catalyzed bis-cyclization of propargyl chlorides and carbonates.
    Inuki S; Yoshimitsu Y; Oishi S; Fujii N; Ohno H
    J Org Chem; 2010 Jun; 75(11):3831-42. PubMed ID: 20455522
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cycloaddition/Ring opening reaction sequences of N-alkenyl aziridines: influence of the aziridine nitrogen on stereoselectivity.
    Siebert MR; Yudin AK; Tantillo DJ
    Org Lett; 2008 Jan; 10(1):57-60. PubMed ID: 18052185
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diastereoselective synthesis of substituted tetrahydrofurans via Prins cyclization of enol ethers.
    Gogoi P; Das VK; Saikia AK
    J Org Chem; 2014 Sep; 79(18):8592-8. PubMed ID: 25185033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Silver(I)-catalyzed dual activation of propargylic alcohol and aziridine/azetidine: triggering ring-opening and endo-selective ring-closing in a cascade.
    Bera M; Roy S
    J Org Chem; 2009 Nov; 74(22):8814-7. PubMed ID: 19831345
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.