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 *

118 related articles for article (PubMed ID: 26952324)

  • 1. From Silylated Trishomoallylic Alcohols to Dioxaspiroundecanes or Oxocanes: Catalyst and Substitution Influence.
    Barbero A; Diez-Varga A; Herrero M; Pulido FJ
    J Org Chem; 2016 Apr; 81(7):2704-12. PubMed ID: 26952324
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Synthesis of Azepane Derivatives by Silyl-aza-Prins Cyclization of Allylsilyl Amines: Influence of the Catalyst in the Outcome of the Reaction.
    Barbero A; Diez-Varga A; Pulido FJ; González-Ortega A
    Org Lett; 2016 May; 18(9):1972-5. PubMed ID: 27074135
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multicomponent prins cyclization from allylsilyl alcohols leading to dioxaspirodecanes.
    Barbero A; Diez-Varga A; Pulido FJ
    Org Lett; 2013 Oct; 15(20):5234-7. PubMed ID: 24090371
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unexpected Domino Silyl-Prins/Aryl Migration Process from Geminal Vinylsilyl Alcohols.
    Díez-Poza C; Barbero A
    Org Lett; 2021 Nov; 23(21):8385-8389. PubMed ID: 34615353
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stereoselective Synthesis of 2,3,5-Trisubstituted Tetrahydrofurans Initiated by a Titanium-BINOLate-Catalyzed Vinylogous Aldol Reaction.
    Hoffmeyer P; Schneider C
    J Org Chem; 2019 Jan; 84(2):1079-1084. PubMed ID: 30575382
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorinated alcohols as promoters for the metal-free direct substitution reaction of allylic alcohols with nitrogenated, silylated, and carbon nucleophiles.
    Trillo P; Baeza A; Nájera C
    J Org Chem; 2012 Sep; 77(17):7344-54. PubMed ID: 22876815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The silylalkyne-Prins cyclization: stereoselective synthesis of tetra- and pentasubstituted halodihydropyrans.
    Miranda PO; Ramírez MA; Martín VS; Padrón JI
    Org Lett; 2006 Apr; 8(8):1633-6. PubMed ID: 16597128
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diastereoselective Synthesis of
    Peña LF; López E; Sánchez-González Á; Barbero A
    Molecules; 2023 Mar; 28(7):. PubMed ID: 37049842
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Stereoselective construction of quaternary carbon stereocenters via a semipinacol rearrangement strategy.
    Wang B; Tu YQ
    Acc Chem Res; 2011 Nov; 44(11):1207-22. PubMed ID: 21728380
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Electrophilic aromatic prenylation via cascade cyclization.
    Kodet JG; Topczewski JJ; Gardner KD; Wiemer DF
    Tetrahedron; 2013 Oct; 69(44):9212-9218. PubMed ID: 24610962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Influence of the Substituents on the Opening of Silylepoxy Alcohols: 5-
    Díez-Poza C; Barbero A
    Molecules; 2021 Dec; 26(23):. PubMed ID: 34885968
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Syntheses of Polycyclic Tetrahydrofurans by Cascade Reactions Consisting of Five-Membered Ring Selective Prins Cyclization and Friedel-Crafts Cyclization.
    Sakata Y; Yasui E; Takatori K; Suzuki Y; Mizukami M; Nagumo S
    J Org Chem; 2018 Aug; 83(16):9103-9118. PubMed ID: 29972019
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Highly selective palladium catalyzed kinetic resolution and enantioselective substitution of racemic allylic carbonates with sulfur nucleophiles: asymmetric synthesis of allylic sulfides, allylic sulfones, and allylic alcohols.
    Gais HJ; Jagusch T; Spalthoff N; Gerhards F; Frank M; Raabe G
    Chemistry; 2003 Sep; 9(17):4202-21. PubMed ID: 12953206
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis of the C22-C26 tetrahydropyran segment of phorboxazole by a stereoselective prins cyclization.
    Rychnovsky SD; Thomas CR
    Org Lett; 2000 May; 2(9):1217-9. PubMed ID: 10810711
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Changing the Reaction Pathway of Silyl-Prins Cyclization by Switching the Lewis Acid: Application to the Synthesis of an Antinociceptive Compound.
    Díez-Poza C; Fernández-Peña L; González-Andrés P; Barbero A
    J Org Chem; 2023 Jun; 88(11):6776-6783. PubMed ID: 37220201
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tandem Prins/Friedel–Crafts cyclization for stereoselective synthesis of heterotricyclic systems.
    Reddy BV; Borkar P; Yadav JS; Sridhar B; Grée R
    J Org Chem; 2011 Oct; 76(19):7677-90. PubMed ID: 21842903
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A tandem Prins spirocyclization for the stereoselective synthesis of tetrahydrospiro[chroman-2,4'-pyran] derivatives.
    Subba Reddy BV; Hanuman Reddy V; Medaboina D; Sridhar B; Rami Reddy YV
    Org Biomol Chem; 2016 Mar; 14(12):3234-7. PubMed ID: 26915773
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.