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 *

153 related articles for article (PubMed ID: 21932228)

  • 1. Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations.
    Crane EA; Zabawa TP; Farmer RL; Scheidt KA
    Angew Chem Int Ed Engl; 2011 Sep; 50(39):9112-5. PubMed ID: 21932228
    [No Abstract]   [Full Text] [Related]  

  • 2. Total synthesis, stereochemical reassignment, and biological evaluation of (-)-lyngbyaloside B.
    Fuwa H; Okuaki Y; Yamagata N; Sasaki M
    Angew Chem Int Ed Engl; 2015 Jan; 54(3):868-73. PubMed ID: 25393532
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Enantioselective synthesis of the C18-C25 segment of lasonolide A by an oxonia-cope prins cascade.
    Dalgard JE; Rychnovsky SD
    Org Lett; 2005 Apr; 7(8):1589-91. PubMed ID: 15816759
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stereoselective synthesis of both tetrahydropyran rings of the antitumor macrolide, (-)-lasonolide A.
    Ghosh AK; Ren GB
    J Org Chem; 2012 Mar; 77(5):2559-65. PubMed ID: 22324913
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stereoselective, Ag-Catalyzed Cyclizations To Access Polysubstituted Pyran Ring Systems: Synthesis of C1-C12 Subunit of Madeirolide A.
    Watanabe K; Li J; Veerasamy N; Ghosh A; Carter RG
    Org Lett; 2016 Apr; 18(8):1744-7. PubMed ID: 27031993
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stereoselective synthesis of C5-C20 and C21-C34 subunits of the core structure of the aplyronines. Applications of enantioselective additions of chiral allenylindium reagents to chiral aldehydes.
    Marshall JA; Johns BA
    J Org Chem; 2000 Mar; 65(5):1501-10. PubMed ID: 10814114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Total synthesis and biological assessment of (-)-exiguolide and analogues.
    Fuwa H; Suzuki T; Kubo H; Yamori T; Sasaki M
    Chemistry; 2011 Feb; 17(9):2678-88. PubMed ID: 21264972
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Total Synthesis of (-)-Exiguolide.
    Zhang Z; Xie H; Li H; Gao L; Song Z
    Org Lett; 2015 Oct; 17(19):4706-9. PubMed ID: 26371396
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stereoselective synthesis of the tetrahydropyran core of polycarvernoside A.
    Barry CS; Bushby N; Harding JR; Willis CL
    Org Lett; 2005 Jun; 7(13):2683-6. PubMed ID: 15957921
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enantioselective syntheses of the proposed structures of cytotoxic macrolides iriomoteolide-1a and -1b.
    Ghosh AK; Yuan H
    Org Lett; 2010 Jul; 12(14):3120-3. PubMed ID: 20560539
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthetic studies on the bryostatins: synthetic routes to analogues containing the tricyclic macrolactone core.
    Keck GE; Truong AP
    Org Lett; 2005 May; 7(11):2153-6. PubMed ID: 15901157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Total synthesis of (+)-18-epi-latrunculol A.
    Williams BD; Smith AB
    Org Lett; 2013 Sep; 15(17):4584-7. PubMed ID: 23972216
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enantioselective reductive coupling of alkynes and alpha-keto aldehydes via rhodium-catalyzed hydrogenation: an approach to bryostatin substructures.
    Cho CW; Krische MJ
    Org Lett; 2006 Mar; 8(5):891-4. PubMed ID: 16494467
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Design, synthesis, and biological evaluation of truncated superstolide A.
    Chen L; Riaz Ahmed KB; Huang P; Jin Z
    Angew Chem Int Ed Engl; 2013 Mar; 52(12):3446-9. PubMed ID: 23404936
    [No Abstract]   [Full Text] [Related]  

  • 15. Enantioselective synthesis of a diastereomer of iriomoteolide-1a. What is the correct structure of the natural product?
    Fang L; Yang J; Yang F
    Org Lett; 2010 Jul; 12(14):3124-7. PubMed ID: 20560543
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Completely OH-selective FeCl3-catalyzed Prins cyclization: highly stereoselective synthesis of 4-OH-tetrahydropyrans.
    Zheng K; Liu X; Qin S; Xie M; Lin L; Hu C; Feng X
    J Am Chem Soc; 2012 Oct; 134(42):17564-73. PubMed ID: 23030638
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New reactions of 2-methylenetetrahydropyrans. A three component coupling protocol for the synthesis of tetrahydropyranyl ketides.
    Liang G; Bateman LJ; Totah NI
    Chem Commun (Camb); 2009 Nov; (42):6457-9. PubMed ID: 19841808
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stereoselective Synthesis of Hexahydro-1H-spiro[isoquinoline-4,4'-pyran] Scaffolds through an Intramolecular Prins Cascade Process.
    Subba Reddy BV; Medaboina D; Sridhar B
    J Org Chem; 2015 Jan; 80(1):653-60. PubMed ID: 25415448
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TMSBr/InBr3-promoted Prins cyclization/homobromination of dienyl alcohol with aldehyde to construct cis-THP containing an exocyclic E-alkene.
    Li L; Sun X; He Y; Gao L; Song Z
    Chem Commun (Camb); 2015 Oct; 51(80):14925-8. PubMed ID: 26303284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stereoselective total synthesis of mucocin, an antitumor agent.
    Takahashi S; Kubota A; Nakata T
    Angew Chem Int Ed Engl; 2002 Dec; 41(24):4751-4. PubMed ID: 12481348
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.