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 *

87 related articles for article (PubMed ID: 24531648)

  • 21. Substituent effects on the iodine-catalyzed thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates: mechanistic studies.
    Chuang TH; Chang WY; Li CF; Wen YC; Tsai CC
    J Org Chem; 2011 Dec; 76(23):9678-86. PubMed ID: 22011143
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Enantioselective organocatalytic intramolecular Diels-Alder reactions: a computational study.
    Duarte FJ; Santos AG
    J Org Chem; 2012 Apr; 77(7):3252-61. PubMed ID: 22364202
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Green protocol for conjugate addition of thiols to alpha,beta-unsaturated ketones using a [bmim]PF6/H2O system.
    Yadav JS; Reddy BV; Baishya G
    J Org Chem; 2003 Sep; 68(18):7098-100. PubMed ID: 12946157
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Palladium pincer complex-catalyzed trimethyltin substitution of functionalized propargylic substrates. An efficient route to propargyl- and allenyl-stannanes.
    Kjellgren J; Sundén H; Szabó KJ
    J Am Chem Soc; 2004 Jan; 126(2):474-5. PubMed ID: 14719938
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Heterogeneous versus homogeneous palladium catalysts for ligandless mizoroki-heck reactions: a comparison of batch/microwave and continuous-flow processing.
    Glasnov TN; Findenig S; Kappe CO
    Chemistry; 2009; 15(4):1001-10. PubMed ID: 19086042
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The efficiency of the metal catalysts in the nucleophilic substitution of alcohols is dependent on the nucleophile and not on the electrophile.
    Biswas S; Samec JS
    Chem Asian J; 2013 May; 8(5):974-81. PubMed ID: 23471850
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Selenium-catalyzed regioselective cyclization of unsaturated carboxylic acids using hypervalent iodine oxidants.
    Singh FV; Wirth T
    Org Lett; 2011 Dec; 13(24):6504-7. PubMed ID: 22085140
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Lanthanum(III) catalysts for highly efficient and chemoselective transesterification.
    Hatano M; Ishihara K
    Chem Commun (Camb); 2013 Mar; 49(20):1983-97. PubMed ID: 23325290
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Direct amidation of carboxylic acids catalyzed by ortho-iodo arylboronic acids: catalyst optimization, scope, and preliminary mechanistic study supporting a peculiar halogen acceleration effect.
    Gernigon N; Al-Zoubi RM; Hall DG
    J Org Chem; 2012 Oct; 77(19):8386-400. PubMed ID: 23013456
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A simple iridium catalyst with a single resolved stereocenter for enantioselective allylic amination. Catalyst selection from mechanistic analysis.
    Leitner A; Shekhar S; Pouy MJ; Hartwig JF
    J Am Chem Soc; 2005 Nov; 127(44):15506-14. PubMed ID: 16262414
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ethynyl benziodoxolones for the direct alkynylation of heterocycles: structural requirement, improved procedure for pyrroles, and insights into the mechanism.
    Brand JP; Chevalley C; Scopelliti R; Waser J
    Chemistry; 2012 Apr; 18(18):5655-66. PubMed ID: 22438043
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Chemoselective synthesis of substituted imines, secondary amines, and beta-amino carbonyl compounds from nitroaromatics through cascade reactions on gold catalysts.
    Santos LL; Serna P; Corma A
    Chemistry; 2009 Aug; 15(33):8196-203. PubMed ID: 19609994
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone.
    Sun J; Dong Y; Cao L; Wang X; Wang S; Hu Y
    J Org Chem; 2004 Dec; 69(25):8932-4. PubMed ID: 15575776
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Efficient synthesis of E-alpha-haloenones through chemoselective alkyne activation over allene with triazole-Au catalysts.
    Wang D; Ye X; Shi X
    Org Lett; 2010 May; 12(9):2088-91. PubMed ID: 20384312
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chiral squaramide-catalyzed highly diastereo- and enantioselective direct Michael addition of nitroalkanes to nitroalkenes.
    Yang W; Du DM
    Chem Commun (Camb); 2011 Dec; 47(47):12706-8. PubMed ID: 22042378
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Regiocontrolled, palladium-catalyzed bisfunctionalization of allenyl esters. Multicomponent coupling approaches to highly substituted alpha,beta-unsaturated delta-lactones.
    Hopkins CD; Guan L; Malinakova HC
    J Org Chem; 2005 Aug; 70(17):6848-62. PubMed ID: 16095305
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Copper(I) catalyzed asymmetric 1,2-addition of Grignard reagents to α-methyl substituted α,β-unsaturated ketones.
    Madduri AV; Minnaard AJ; Harutyunyan SR
    Chem Commun (Camb); 2012 Feb; 48(10):1478-80. PubMed ID: 22124420
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Iodine catalyzed one-pot multicomponent synthesis of a library of compounds containing tetrazolo[1,5-a]pyrimidine core.
    Zeng LY; Cai C
    J Comb Chem; 2010; 12(1):35-40. PubMed ID: 19950908
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 1,2,3-triazole bound Au(I) (TA-Au) as chemoselective catalysts in promoting asymmetric synthesis of substituted allenes.
    Wang D; Gautam LN; Bollinger C; Harris A; Li M; Shi X
    Org Lett; 2011 May; 13(10):2618-21. PubMed ID: 21504205
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Chiral recyclable dimeric and polymeric Cr(III) salen complexes catalyzed aminolytic kinetic resolution of trans-aromatic epoxides under microwave irradiation.
    Kureshy RI; Prathap KJ; Singh S; Agrawal S; Khan NU; Abdi SH; Jasra RV
    Chirality; 2007 Nov; 19(10):809-15. PubMed ID: 17786914
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.