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 *

126 related articles for article (PubMed ID: 28244753)

  • 1. Tuning the Stability and the Reactivity of Substituted [3]Dendralenes for Quick Access to Diverse Copiously Functionalized Fused Polycycles with Step and Atom Economy.
    Naidu GS; Singh R; Kumar M; Ghosh SK
    J Org Chem; 2017 Apr; 82(7):3648-3658. PubMed ID: 28244753
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diene-Transmissive Diels-Alder Sequences with Benzynes.
    George J; Ward JS; Sherburn MS
    Org Lett; 2019 Sep; 21(18):7529-7533. PubMed ID: 31479273
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multicomponent Diene-Transmissive Diels-Alder Sequences Featuring Aminodendralenes.
    Tan SM; Willis AC; Paddon-Row MN; Sherburn MS
    Angew Chem Int Ed Engl; 2016 Feb; 55(9):3081-5. PubMed ID: 26823233
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ruthenium-catalyzed synthesis of 2,3-cyclo[3]dendralenes and complex polycycles from propargyl alcohols.
    Thies N; Haak E
    Angew Chem Int Ed Engl; 2015 Mar; 54(13):4097-101. PubMed ID: 25655395
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diene-Transmissive Enantioselective Diels-Alder Reactions and Sequences Involving Substituted Dendralenes.
    George J; Sherburn MS
    J Org Chem; 2019 Nov; 84(22):14712-14723. PubMed ID: 31614081
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Preparation and synthetic value of π-bond-rich branched hydrocarbons.
    Sherburn MS
    Acc Chem Res; 2015 Jul; 48(7):1961-70. PubMed ID: 26151489
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dendralenes branch out: cross-conjugated oligoenes allow the rapid generation of molecular complexity.
    Hopf H; Sherburn MS
    Angew Chem Int Ed Engl; 2012 Mar; 51(10):2298-338. PubMed ID: 22337341
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cross-coupling for cross-conjugation: practical synthesis and Diels-Alder reactions of [3]dendralenes.
    Bradford TA; Payne AD; Willis AC; Paddon-Row MN; Sherburn MS
    Org Lett; 2007 Nov; 9(23):4861-4. PubMed ID: 17929828
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diversity-Oriented Approaches to Polycyclics and Bioinspired Molecules via the Diels-Alder Strategy: Green Chemistry, Synthetic Economy, and Beyond.
    Kotha S; Chavan AS; Goyal D
    ACS Comb Sci; 2015 May; 17(5):253-302. PubMed ID: 25875156
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enantioselective oxa-Diels-Alder Sequences of Dendralenes.
    Fan YM; Yu LJ; Gardiner MG; Coote ML; Sherburn MS
    Angew Chem Int Ed Engl; 2022 Sep; 61(39):e202204872. PubMed ID: 35900232
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis and Diels-Alder Reactivity of Substituted [4]Dendralenes.
    Saglam MF; Alborzi AR; Payne AD; Willis AC; Paddon-Row MN; Sherburn MS
    J Org Chem; 2016 Feb; 81(4):1461-75. PubMed ID: 26757131
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Rapid Aza-Bicycle Synthesis from Dendralenes and Imines.
    Fan YM; George J; Wang JYJ; Gardiner MG; Coote ML; Sherburn MS
    Org Lett; 2023 Oct; 25(41):7545-7550. PubMed ID: 37801309
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A general synthesis of dendralenes.
    George J; Ward JS; Sherburn MS
    Chem Sci; 2019 Nov; 10(43):9969-9973. PubMed ID: 32055353
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis of Functionalized [3], [4], [5] and [6]Dendralenes through Palladium-Catalyzed Cross-Couplings of Substituted Allenoates.
    Lippincott DJ; Linstadt RT; Maser MR; Lipshutz BH
    Angew Chem Int Ed Engl; 2017 Jan; 56(3):847-850. PubMed ID: 27936307
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A General Stereoselective Synthesis of [4]Dendralenes.
    Fan YM; Sowden MJ; Magann NL; Lindeboom EJ; Gardiner MG; Sherburn MS
    J Am Chem Soc; 2022 Nov; 144(43):20090-20098. PubMed ID: 36260914
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nitroso-dienophile additions to dendralenes: a short synthesis of branched aminosugars.
    Wang R; Bojase G; Willis AC; Paddon-Row MN; Sherburn MS
    Org Lett; 2012 Nov; 14(22):5652-5. PubMed ID: 23106239
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multicomponent Double Diels-Alder/Nazarov Tandem Cyclization of Symmetric Cross-Conjugated Diynones to Generate [6-5-6] Tricyclic Products.
    Carmichael RA; Chalifoux WA
    Chemistry; 2016 Jun; 22(26):8781-5. PubMed ID: 27124516
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stereo-controlled synthesis of polyheterocycles via the diene-transmissive hetero-Diels-Alder reaction of β,γ-unsaturated α-keto esters.
    Otani T; Tamai Y; Seki K; Kikuchi T; Miyazawa T; Saito T
    Org Biomol Chem; 2015 Jun; 13(21):5875-9. PubMed ID: 25920697
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tandem Bond-Forming Reactions of 1-Alkynyl Ethers.
    Minehan TG
    Acc Chem Res; 2016 Jun; 49(6):1168-81. PubMed ID: 27195605
    [TBL] [Abstract][Full Text] [Related]  

  • 20. (1R)-(+)-camphor and acetone derived alpha'-hydroxy enones in asymmetric Diels-Alder reaction: catalytic activation by Lewis and Brønsted acids, substrate scope, applications in syntheses, and mechanistic studies.
    Bañuelos P; García JM; Gómez-Bengoa E; Herrero A; Odriozola JM; Oiarbide M; Palomo C; Razkin J
    J Org Chem; 2010 Mar; 75(5):1458-73. PubMed ID: 20121243
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.