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 *

123 related articles for article (PubMed ID: 24057350)

  • 1. Visible-light-induced, copper(I)-catalysed C-N coupling between o-phenylenediamine and terminal alkynes: one-pot synthesis of 3-phenyl-2-hydroxy-quinoxalines.
    Sagadevan A; Ragupathi A; Hwang KC
    Photochem Photobiol Sci; 2013 Dec; 12(12):2110-8. PubMed ID: 24057350
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copper catalyzed photoredox synthesis of α-keto esters, quinoxaline, and naphthoquinone: controlled oxidation of terminal alkynes to glyoxals.
    Das DK; Kumar Pampana VK; Hwang KC
    Chem Sci; 2018 Oct; 9(37):7318-7326. PubMed ID: 30294421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Visible light initiated amino group ortho-directed copper(i)-catalysed aerobic oxidative C(sp)-S coupling reaction: synthesis of substituted 2-phenylbenzothiazoles via thia-Wolff rearrangement.
    Reddy MB; Anandhan R
    Chem Commun (Camb); 2020 Mar; 56(26):3781-3784. PubMed ID: 32129436
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copper-catalyzed synthesis of quinoxalines with o-phenylenediamine and terminal alkyne in the presence of bases.
    Wang W; Shen Y; Meng X; Zhao M; Chen Y; Chen B
    Org Lett; 2011 Sep; 13(17):4514-7. PubMed ID: 21805970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copper(i)-catalysed oxidative C-N coupling of 2-aminopyridine with terminal alkynes featuring a C[triple bond, length as m-dash]C bond cleavage promoted by visible light.
    Ragupathi A; Sagadevan A; Lin CC; Hwu JR; Hwang KC
    Chem Commun (Camb); 2016 Sep; 52(79):11756-11759. PubMed ID: 27709172
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Photoinduced Copper-Catalyzed Regioselective Synthesis of Indoles: Three-Component Coupling of Arylamines, Terminal Alkynes, and Quinones.
    Sagadevan A; Ragupathi A; Hwang KC
    Angew Chem Int Ed Engl; 2015 Nov; 54(47):13896-901. PubMed ID: 26338043
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copper-catalyzed aerobic oxidative coupling of o-phenylenediamines with 2-aryl/heteroarylethylamines: direct access to construct quinoxalines.
    Gopalaiah K; Saini A; Chandrudu SN; Rao DC; Yadav H; Kumar B
    Org Biomol Chem; 2017 Mar; 15(10):2259-2268. PubMed ID: 28240337
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Operationally simple copper-promoted coupling of terminal alkynes with benzyl halides.
    Davies KA; Abel RC; Wulff JE
    J Org Chem; 2009 May; 74(10):3997-4000. PubMed ID: 19422268
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypervalent iodine(III)-induced oxidative [4+2] annulation of o-phenylenediamines and electron-deficient alkynes: direct synthesis of quinoxalines from alkyne substrates under metal-free conditions.
    Okumura S; Takeda Y; Kiyokawa K; Minakata S
    Chem Commun (Camb); 2013 Oct; 49(81):9266-8. PubMed ID: 23995675
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A one-pot procedure for the regiocontrolled synthesis of allyltriazoles via the Pd-Cu bimetallic catalyzed three-component coupling reaction of nonactivated terminal alkynes, allyl carbonate, and trimethylsilyl azide.
    Kamijo S; Jin T; Huo Z; Yamamoto Y
    J Org Chem; 2004 Apr; 69(7):2386-93. PubMed ID: 15049635
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DABCO-Catalyzed DMSO-Promoted Sulfurative 1,2-Diamination of Phenylacetylenes with Elemental Sulfur and
    Tran TMC; Lai ND; Bui TTT; Mac DH; Nguyen TTT; Retailleau P; Nguyen TB
    Org Lett; 2023 Oct; 25(39):7225-7229. PubMed ID: 37738043
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes.
    Cox RJ; Ritson DJ; Dane TA; Berge J; Charmant JP; Kantacha A
    Chem Commun (Camb); 2005 Feb; (8):1037-9. PubMed ID: 15719108
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Indole synthesis by conjugate addition of anilines to activated acetylenes and an unusual ligand-free copper(II)-mediated intramolecular cross-coupling.
    Gao D; Back TG
    Chemistry; 2012 Nov; 18(46):14828-40. PubMed ID: 23019064
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Benzofuran and indole synthesis via Cu(I)-catalyzed coupling of N-tosylhydrazone and o-hydroxy or o-amino phenylacetylene.
    Xiao T; Dong X; Zhou L
    Org Biomol Chem; 2013 Mar; 11(9):1490-7. PubMed ID: 23184182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Copper-catalysed Csp
    Zhao B; Wu Y; Yuan Y; Shi Z
    Chem Commun (Camb); 2020 Apr; 56(34):4676-4679. PubMed ID: 32211642
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Base-catalyzed multicomponent access to quinoxalin-2-thiones from
    Nguyen TB; Mac DH; Tran TMC; Nguyen BN; Cao HT
    Org Biomol Chem; 2022 Sep; 20(36):7226-7231. PubMed ID: 36053547
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis of N-arylated 1,2-dihydroheteroaromatics through the three-component reaction of arynes with N-heteroaromatics and terminal alkynes or ketones.
    Jeganmohan M; Bhuvaneswari S; Cheng CH
    Chem Asian J; 2010 Jan; 5(1):153-9. PubMed ID: 20013994
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Copper-catalyzed coupling reaction of C-OMe bonds adjacent to a nitrogen atom with terminal alkynes.
    Yao B; Zhang Y; Li Y
    J Org Chem; 2010 Jul; 75(13):4554-61. PubMed ID: 20536252
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Propargyl amine synthesis catalysed by gold and copper thin films by using microwave-assisted continuous-flow organic synthesis (MACOS).
    Shore G; Yoo WJ; Li CJ; Organ MG
    Chemistry; 2010 Jan; 16(1):126-33. PubMed ID: 19950339
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A one-pot coupling-addition-cyclocondensation sequence (CACS) to 2-substituted 3-acylpyrroles initiated by a copper-free alkynylation.
    Nordmann J; Müller TJ
    Org Biomol Chem; 2013 Oct; 11(38):6556-61. PubMed ID: 23982686
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.