BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 25200563)

  • 1. Silyl enol ether Prins cyclization: diastereoselective formation of substituted tetrahydropyran-4-ones.
    Tay GC; Huang CY; Rychnovsky SD
    J Org Chem; 2014 Sep; 79(18):8733-49. PubMed ID: 25200563
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oxonia-cope prins cyclizations: a facile method for the synthesis of tetrahydropyranones bearing quaternary centers.
    Dalgard JE; Rychnovsky SD
    J Am Chem Soc; 2004 Dec; 126(48):15662-3. PubMed ID: 15571386
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diastereoselective synthesis of dihydropyrans via Prins cyclization of enol ethers: total asymmetric synthesis of (+)-civet cat compound.
    Sultana S; Indukuri K; Deka MJ; Saikia AK
    J Org Chem; 2013 Dec; 78(23):12182-8. PubMed ID: 24245586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prins cyclizations in silyl additives with suppression of epimerization: versatile tool in the synthesis of the tetrahydropyran backbone of natural products.
    Chan KP; Loh TP
    Org Lett; 2005 Sep; 7(20):4491-4. PubMed ID: 16178566
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Unique diastereoselectivity trends in aminyl radical cyclizations onto silyl enol ethers.
    Zlotorzynska M; Zhai H; Sammis GM
    J Org Chem; 2010 Feb; 75(3):864-72. PubMed ID: 20043630
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Asymmetric Electrophilic α-Amination of Silyl Enol Ether Derivatives via the Nitrosocarbonyl Hetero-ene Reaction.
    Sandoval D; Samoshin AV; Read de Alaniz J
    Org Lett; 2015 Sep; 17(18):4514-7. PubMed ID: 26317504
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prins cyclization of bis(silyl) homoallylic alcohols to form 2,6-cis-tetrahydropyrans containing a geometrically defined exocyclic vinylsilane: efficient synthesis of ring B of the bryostatins.
    Lu J; Song Z; Zhang Y; Gan Z; Li H
    Angew Chem Int Ed Engl; 2012 May; 51(22):5367-70. PubMed ID: 22504783
    [No Abstract]   [Full Text] [Related]  

  • 9. Acid-promoted Prins cyclizations of enol ethers to form tetrahydropyrans.
    Hart DJ; Bennett CE
    Org Lett; 2003 May; 5(9):1499-502. PubMed ID: 12713308
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hydroxyl-substituted ladder polyethers via selective tandem epoxidation/cyclization sequence.
    Czabaniuk LC; Jamison TF
    Org Lett; 2015 Feb; 17(4):774-7. PubMed ID: 25647091
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An environmentally benign synthesis of cis-2,6-disubstituted tetrahydropyrans via indium-mediated tandem allylation/Prins cyclization reaction.
    Pham M; Allatabakhsh A; Minehan TG
    J Org Chem; 2008 Jan; 73(2):741-4. PubMed ID: 18095701
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis of Polysubstituted Tetrahydropyrans by Stereoselective Hydroalkoxylation of Silyl Alkenols: En Route to Tetrahydropyranyl Marine Analogues.
    Díez-Poza C; Val P; Pulido FJ; Barbero A
    Mar Drugs; 2018 Nov; 16(11):. PubMed ID: 30388761
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enantio- and diastereoselective assembly of tetrahydrofuran and tetrahydropyran skeletons with all-carbon-substituted quaternary stereocenters.
    Chen Z; Sun J
    Angew Chem Int Ed Engl; 2013 Dec; 52(51):13593-6. PubMed ID: 24254193
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis of the C20-C32 tetrahydropyran core of the phorboxazoles and the C22 epimer via a stereodivergent Michael reaction.
    Clarke PA; Ermanis K
    Org Lett; 2012 Nov; 14(21):5550-3. PubMed ID: 23088315
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stereoselective Synthesis of Highly Substituted Tetrahydropyrans through an Evans Aldol-Prins Strategy.
    Álvarez-Méndez SJ; Fariña-Ramos M; Villalba ML; Perretti MD; García C; Moujir LM; Ramírez MA; Martín VS
    J Org Chem; 2018 Aug; 83(16):9039-9066. PubMed ID: 30036470
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The role of asynchronous bond formation in the diastereoselective epoxidation of cyclic enol ethers: a density functional theory study.
    Orendt AM; Roberts SW; Rainier JD
    J Org Chem; 2006 Jul; 71(15):5565-73. PubMed ID: 16839135
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Design, Prins-cyclization reaction promoting diastereoselective synthesis of 10 new tetrahydropyran derivatives and in vivo antinociceptive evaluations.
    Capim SL; Carneiro PH; Castro PC; Barros MR; Marinho BG; Vasconcellos ML
    Eur J Med Chem; 2012 Dec; 58():1-11. PubMed ID: 23085140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Formation of highly substituted tetrahydropyranones: application to the total synthesis of cyanolide A.
    Tay GC; Gesinski MR; Rychnovsky SD
    Org Lett; 2013 Sep; 15(17):4536-9. PubMed ID: 23962271
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gold(I)-catalyzed cyclizations of silyl enol ethers: application to the synthesis of (+)-lycopladine A.
    Staben ST; Kennedy-Smith JJ; Huang D; Corkey BK; Lalonde RL; Toste FD
    Angew Chem Int Ed Engl; 2006 Sep; 45(36):5991-4. PubMed ID: 16888820
    [No Abstract]   [Full Text] [Related]  

  • 20. Stereoselective Synthesis of Substituted Tetrahydropyrans and Isochromans by Cyclization of Phenylseleno Alcohols.
    Temperini A; Barattucci A; Bonaccorsi PM; Rosati O; Minuti L
    J Org Chem; 2015 Aug; 80(16):8102-12. PubMed ID: 26218823
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.