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 *

616 related articles for article (PubMed ID: 18095701)

  • 1. 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]  

  • 2. Enantioselective synthesis of 2,6-cis-disubstituted tetrahydropyrans via a tandem catalytic asymmetric hydrogenation/oxa-Michael cyclization: an efficient approach to (-)-centrolobine.
    Xie JH; Guo LC; Yang XH; Wang LX; Zhou QL
    Org Lett; 2012 Sep; 14(18):4758-61. PubMed ID: 22934577
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Enantioselective construction of cis-2,6-disubstituted dihydropyrans: total synthesis of (-)-centrolobine.
    Chaładaj W; Kowalczyk R; Jurczak J
    J Org Chem; 2010 Mar; 75(5):1740-3. PubMed ID: 20112973
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. One-pot synthesis and SAR study of cis-2,6-dialkyl-4-chloro-tetrahydropyrans.
    Miranda PO; León LG; Martín VS; Padrón JI; Padrón JM
    Bioorg Med Chem Lett; 2006 Jun; 16(12):3135-8. PubMed ID: 16603350
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diastereoselective synthesis of substituted tetrahydrothiophenes and -thiopyrans via thia-Prins cyclization reaction.
    Borah M; Gogoi P; Indukuri K; Saikia AK
    J Org Chem; 2015 Mar; 80(5):2641-8. PubMed ID: 25674813
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthetic and mechanistic studies of indium-mediated allylation of imines in ionic liquids.
    Law MC; Cheung TW; Wong KY; Chan TH
    J Org Chem; 2007 Feb; 72(3):923-9. PubMed ID: 17253812
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diastereoselective synthesis of substituted dihydropyrans via an oxonium-ene cyclization reaction.
    Saha P; Ghosh P; Sultana S; Saikia AK
    Org Biomol Chem; 2012 Nov; 10(43):8730-8. PubMed ID: 23037969
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Green chemistry: solvent- and metal-free Prins cyclization. Application to sequential reactions.
    Clarisse D; Pelotier B; Piva O; Fache F
    Chem Commun (Camb); 2012 Jan; 48(1):157-9. PubMed ID: 22068454
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Competitive silyl-Prins cyclization versus tandem Sakurai-Prins cyclization: an interesting substitution effect.
    Diez-Varga A; Barbero H; Pulido FJ; González-Ortega A; Barbero A
    Chemistry; 2014 Oct; 20(43):14112-9. PubMed ID: 25196494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Solid phase synthesis of highly substituted tetrahydropyrans by tandem ene-reaction/intramolecular Sakurai cyclization.
    Broussy S; Waldmann H
    J Comb Chem; 2007; 9(6):1138-43. PubMed ID: 17935301
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Use of allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3-, C4-, and C5-carbon sources: palladium-catalyzed allylation of aldehydes.
    Shimizu M; Kimura M; Tamaru Y
    Chemistry; 2005 Nov; 11(22):6629-42. PubMed ID: 16130159
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Formal [4 + 2] cycloaddition of donor-acceptor cyclobutanes and aldehydes: stereoselective access to substituted tetrahydropyrans.
    Parsons AT; Johnson JS
    J Am Chem Soc; 2009 Oct; 131(40):14202-3. PubMed ID: 19764759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Stereoselective construction of 2,6-cis-disubstituted tetrahydropyrans via intramolecular amide enolate alkylation: total synthesis of (-)-centrolobine.
    Latif M; Yun JI; Seshadri K; Kim HR; Park CH; Park H; Kim H; Lee J
    J Org Chem; 2015 Mar; 80(6):3315-20. PubMed ID: 25723100
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The stereoselective synthesis of cis-/trans-fused hexahydropyrano[4,3-b]chromenes via Prins cyclization trapping by a tethered nucleophile.
    Reddy BV; Jalal S; Borkar P; Yadav JS; Reddy PP; Kunwar AC; Sridhar B
    Org Biomol Chem; 2012 Aug; 10(32):6562-8. PubMed ID: 22763607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Palladium-catalyzed stereospecific synthesis of 2,6-disubstituted tetrahydropyrans: 1,3-chirality transfer by an intramolecular oxypalladation reaction.
    Kawai N; Lagrange JM; Ohmi M; Uenishi J
    J Org Chem; 2006 Jun; 71(12):4530-7. PubMed ID: 16749785
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Thia-prins bicyclization approach for the stereoselective synthesis of dithia- and azathia-bicycles.
    Reddy BV; Venkateswarlu A; Borkar P; Yadav JS; Kanakaraju M; Kunwar AC; Sridhar B
    J Org Chem; 2013 Jun; 78(12):6303-8. PubMed ID: 23679080
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 31.