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 *

115 related articles for article (PubMed ID: 26303284)

  • 1. 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]  

  • 2. 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]  

  • 3. 1,4-Hydroiodination of dienyl alcohols with TMSI to form homoallylic alcohols containing a multisubstituted Z-alkene and application to Prins cyclization.
    Xu Y; Yin Z; Lin X; Gan Z; He Y; Gao L; Song Z
    Org Lett; 2015 Apr; 17(8):1846-9. PubMed ID: 25825952
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Mechanistic and computational studies of exocyclic stereocontrol in the synthesis of bryostatin-like cis-2,6-disubstituted 4-alkylidenetetrahydropyrans by Prins cyclization.
    Ogawa Y; Painter PP; Tantillo DJ; Wender PA
    J Org Chem; 2013 Jan; 78(1):104-15. PubMed ID: 23121542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Factors controlling the alkyne prins cyclization: the stability of dihydropyranyl cations.
    Miranda PO; Ramírez MA; Martín VS; Padrón JI
    Chemistry; 2008; 14(20):6260-8. PubMed ID: 18512867
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds.
    Reddy BV; Gopal Reddy S; Ramana Reddy M; Pal Bhadra M; Sarma AV
    Org Biomol Chem; 2014 Oct; 12(37):7257-60. PubMed ID: 25103114
    [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. 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]  

  • 13. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes.
    Reddy KR; Rosa IM; Doriguetto AC; Bastos EL; Silva LF
    Molecules; 2013 Sep; 18(9):11100-30. PubMed ID: 24025458
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Stereoselective synthesis of hexahydro-1H-pyrano- and thiopyrano[3,4-c]quinoline derivatives through a Prins cascade cyclization.
    Reddy BV; Medaboina D; Sridhar B; Singarapu KK
    J Org Chem; 2013 Aug; 78(16):8161-8. PubMed ID: 23859007
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Diastereo- and enantioselective synthesis of 1,3,5,7-tetraol structural units using a Prins cyclisation-reductive cleavage sequence.
    Brun E; Bellosta V; Cossy J
    Chem Commun (Camb); 2014 Jun; 50(51):6718-21. PubMed ID: 24828441
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 2-Arylcyclopropylmethanol as a substitute for homoallyl aryl alcohol in the construction of cis-2,6-disubstituted tetrahydropyran: synthesis of (±)-centrolobine.
    Yadav VK; Verma AK; Kumar P; Hulikal V
    Chem Commun (Camb); 2014 Dec; 50(97):15457-60. PubMed ID: 25354489
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stereoselectivity and regioselectivity in the segment-coupling Prins cyclization.
    Jaber JJ; Mitsui K; Rychnovsky SD
    J Org Chem; 2001 Jun; 66(13):4679-86. PubMed ID: 11421792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.