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 *

160 related articles for article (PubMed ID: 26190818)

  • 1. An Arylative Ring Expansion Cascade of Fused Cyclobutenes via Short-Lived Intermediates with Planar Chirality.
    Arichi N; Yamada K; Yamaoka Y; Takasu K
    J Am Chem Soc; 2015 Aug; 137(30):9579-82. PubMed ID: 26190818
    [TBL] [Abstract][Full Text] [Related]  

  • 2. AlCl₃-Catalyzed Ring Expansion Cascades of Bicyclic Cyclobutenamides Involving Highly Strained Cis,Trans-Cycloheptadienone Intermediates.
    Wang XN; Krenske EH; Johnston RC; Houk KN; Hsung RP
    J Am Chem Soc; 2015 Apr; 137(16):5596-601. PubMed ID: 25895058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A catalytic diastereoselective formal [5+2] cycloaddition approach to azepino[1,2-a]indoles: putative donor-acceptor cyclobutanes as reactive intermediates.
    Shenje R; Martin MC; France S
    Angew Chem Int Ed Engl; 2014 Dec; 53(50):13907-11. PubMed ID: 25339510
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The profound effect of the ring size in the electrocyclic opening of cyclobutene-fused bicyclic systems.
    Ralph MJ; Harrowven DC; Gaulier S; Ng S; Booker-Milburn KI
    Angew Chem Int Ed Engl; 2015 Jan; 54(5):1527-31. PubMed ID: 25483597
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis of chiral cyclobutanes via rhodium/diene-catalyzed asymmetric 1,4-addition: a dramatic ligand effect on the diastereoselectivity.
    Chen YJ; Hu TJ; Feng CG; Lin GQ
    Chem Commun (Camb); 2015 May; 51(42):8773-6. PubMed ID: 25912603
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Thermodynamic control of the electrocyclic ring opening of cyclobutenes: C=X substituents at C-3 mask the kinetic torquoselectivity.
    Um JM; Xu H; Houk KN; Tang W
    J Am Chem Soc; 2009 May; 131(19):6664-5. PubMed ID: 19402639
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones.
    Zhong X; Li Y; Zhang J; Zhang WX; Wang SX; Han FS
    Chem Commun (Camb); 2014 Oct; 50(76):11181-4. PubMed ID: 25111870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An organocatalytic [3+2] cyclisation strategy for the highly enantioselective synthesis of spirooxindoles.
    Voituriez A; Pinto N; Neel M; Retailleau P; Marinetti A
    Chemistry; 2010 Nov; 16(42):12541-4. PubMed ID: 20853298
    [No Abstract]   [Full Text] [Related]  

  • 9. Controllable [2+2] cycloadditions of 1,5-bisallenyl-substituted compounds.
    Jiang X; Cheng X; Ma S
    Angew Chem Int Ed Engl; 2006 Dec; 45(47):8009-13. PubMed ID: 17083138
    [No Abstract]   [Full Text] [Related]  

  • 10. Asymmetric synthesis of 3,3'-spirooxindoles fused with cyclobutanes through organocatalytic formal [2 + 2] cycloadditions under H-bond-directing dienamine activation.
    Qi LW; Yang Y; Gui YY; Zhang Y; Chen F; Tian F; Peng L; Wang LX
    Org Lett; 2014 Dec; 16(24):6436-9. PubMed ID: 25494171
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis of polyfluoroalkyl cyclobutenes from 3-aza-1,5-enynes via an aza-Claisen rearrangement/cyclization cascade.
    Xin X; Wang D; Wu F; Wang C; Wang H; Li X; Wan B
    Org Lett; 2013 Sep; 15(17):4512-5. PubMed ID: 23967800
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pd(0)-catalyzed tandem deprotection/cyclization of tetrahydro-β-carbolines on allenes: application to the synthesis of indolo[2,3-a]quinolizidines.
    Gobé V; Guinchard X
    Org Lett; 2014 Apr; 16(7):1924-7. PubMed ID: 24661091
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Direct synthesis of fused indoles by gold-catalyzed cascade cyclization of diynes.
    Hirano K; Inaba Y; Takahashi N; Shimano M; Oishi S; Fujii N; Ohno H
    J Org Chem; 2011 Mar; 76(5):1212-27. PubMed ID: 21250725
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis of Functionalized Medium-Sized trans-Cycloalkenes by 4π Electrocyclic Ring Opening/Alkylation Sequence.
    Ito T; Tsutsumi M; Yamada KI; Takikawa H; Yamaoka Y; Takasu K
    Angew Chem Int Ed Engl; 2019 Aug; 58(34):11836-11840. PubMed ID: 31259460
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stereoselective spirolactam synthesis via palladium catalyzed arylative allene carbocyclization cascades.
    Li M; Dixon DJ
    Org Lett; 2010 Sep; 12(17):3784-7. PubMed ID: 20698485
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gold(I)-catalyzed, highly diastereoselective, tandem heterocyclizations/[3+2] cycloadditions: synthesis of highly substituted cyclopenta[c]furans.
    Gao H; Wu X; Zhang J
    Chemistry; 2011 Mar; 17(10):2838-41. PubMed ID: 21294202
    [No Abstract]   [Full Text] [Related]  

  • 17. A theoretical study of cyclohexyne addition to carbonyl-Cα bonds: allowed and forbidden electrocyclic and nonpericyclic ring-openings of strained cyclobutenes.
    Sader CA; Houk KN
    J Org Chem; 2012 Jun; 77(11):4939-48. PubMed ID: 22537557
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acid-promoted cascade cyclization to produce fused-polycyclic indole derivatives.
    Yokosaka T; Nakayama H; Nemoto T; Hamada Y
    Org Lett; 2013 Jun; 15(12):2978-81. PubMed ID: 23745602
    [TBL] [Abstract][Full Text] [Related]  

  • 19. From Stereodefined Cyclobutenes to Dienes: Total Syntheses of Ieodomycin D and the Southern Fragment of Macrolactin A.
    Souris C; Misale A; Chen Y; Luparia M; Maulide N
    Org Lett; 2015 Sep; 17(18):4486-9. PubMed ID: 26349917
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Access to indole- and pyrrole-fused diketopiperazines via tandem Ugi-4CR/intramolecular cyclization and its regioselective ring-opening by intermolecular transamidation.
    Pandey S; Khan S; Singh A; Gauniyal HM; Kumar B; Chauhan PM
    J Org Chem; 2012 Nov; 77(22):10211-27. PubMed ID: 23061967
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.